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AU2017360168B2 - Novel anti-human MUC1 antibody Fab fragment - Google Patents

Novel anti-human MUC1 antibody Fab fragment Download PDF

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Publication number
AU2017360168B2
AU2017360168B2 AU2017360168A AU2017360168A AU2017360168B2 AU 2017360168 B2 AU2017360168 B2 AU 2017360168B2 AU 2017360168 A AU2017360168 A AU 2017360168A AU 2017360168 A AU2017360168 A AU 2017360168A AU 2017360168 B2 AU2017360168 B2 AU 2017360168B2
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AU
Australia
Prior art keywords
fab fragment
human
conjugate
seq
human muc1
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AU2017360168A
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AU2017360168A1 (en
Inventor
Hitoshi Doihara
Kazunori HIRAYAMA
Naomi Hosogai
Akifumi Morinaka
Hiroki Shirai
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Astellas Pharma Inc
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Astellas Pharma Inc
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    • G01N2333/47—Assays involving proteins of known structure or function as defined in the subgroups
    • G01N2333/4701—Details
    • G01N2333/4725—Mucins, e.g. human intestinal mucin

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Abstract

[Problem] To provide an anti-human MUC1 antibody Fab fragment, which is expected to be useful for the diagnosis and/or treatment of cancer, particularly the diagnosis and/or treatment of breast cancer or bladder cancer, and a diagnosis means and/or a therapeutic means using a complex containing the Fab fragment. [Solution] An anti-human MUC1 antibody Fab fragment which contains a heavy chain fragment containing a heavy-chain variable region comprising the amino acid sequence represented by SEQ ID NO: 8 or 10, and a light chain containing a light-chain variable region comprising the amino acid sequence represented by SEQ ID NO: 12; and a complex containing the Fab fragment.

Description

DESCRIPTION NOVEL ANTI-HUMAN MUC ANTIBODY FAB FRAGMENT TECHNICAL FIELD
[0001] The present invention relates to a novel anti-human MUCl antibody Fab fragment.
The present invention also relates to a composition for diagnosis and/or for treatment
comprising the anti-human MUC1 antibody Fab fragment, and a method for diagnosing
and/or treating a cancer using the Fab fragment.
BACKGROUND ART
[0002] Mucin 1 (MUC1) is amembrane-bound glycoprotein that is expressed on the lumen
side of epithelial cells constituting the epithelial tissues of the mammary gland, the trachea
and the gastrointestinal tract, etc. (Nat. Rev. Cancer, 2004 Jan; 4 (1): 45-60). MUC1 is
overexpressed in cancer cells of breast cancer (Mod. Pathol., 2005 Oct; 18 (10): 1295-304),
lung cancer (Hum. Pathol., 2008 Jan; 39 (1): 126-36), colorectal cancer (Int. J. Oncol., 2000
Jan; 16 (1): 55-64), bladder cancer (PLoS One, 2014 Mar; 9 (3): e92742), skin cancer
(Histopathology, 2000 Sep; 37 (3): 218-23), thyroid gland cancer (J. Pathol., 2003 Jul; 200
(3): 357-69), stomach cancer (J. Pathol., 2000 Mar; 190 (4): 437-43), pancreatic cancer (Int.
J. Oncol., 2004 Jan; 24 (1): 107-13), kidney cancer (Mod. Pathol., 2004 Feb; 17 (2): 180-8),
ovary cancer (Gynecol. Oncol., 2007 Jun; 105 (3): 695-702) and uterine cervical cancer (Am.
J. Clin. Pathol., 2004 Jul; 122 (1): 61-9), etc. MUCi is useful as a target molecule for
detecting a cancer focus (Nat. Rev. Cancer, 2004 Jan; 4 (1): 45-60; and Pathol. Res. Pract.,
2010 Aug 15; 206 (8): 585-9).
[0003] MUCI undergoes the O-glycosylation of threonine at position 9 of a 20-amino acid
tandem repeat sequence HGVTSAPDTRPAPGSTAPPA (SEQ ID NO: 15) present in an
extracellular domain. In cancer cells, this O-glycosylation is incomplete, and 0
glycosylation such as T(Galp l-3GaNAcal-O-Ser/Thr), Tn(GaNAcaI-O-Ser/Thr) and
2,3ST(Neu5Acc2-3Gal1-3GalNAc-O-Ser/Thr) is known to occur in a cancer-specific
manner (PTL 1 andNPL 1). Since MUCI in normal tissues does not undergo such cancer- specific O-glycosylation, human cancer-specific MUC1 is particularly useful as a target molecule for treating various cancers in humans.
[0004] For example, a 1B2 antibody (PTL 1), a PankoMab antibody (NPL 2), and a 5E5
antibody (PTL 2) are known as antibodies against such human cancer-specific MUC1.
Among these antibodies, the 1B2 antibody has been reported to have high specificity for
human cancer-specific MUC1 as compared with the PankoMab antibody (PTL 1). Ithas
also been reported that the dissociation constant of the 1B2 antibody is 3.7 x 10-10 M (PTL
1), and the dissociation constant of the 5E5 antibody is 1.7 x 10-' M (NPL 1).
[0005] Meanwhile, there are also great needs for the visualization of cancer lesion. First,
there are the needs for the early detection of cancer lesion. Current diagnostic'modalities
such as X-ray photography, echography, computed tomography (CT), magnetic resonance
imaging (MRI), positron emission tomography (PET), and single photon emission computed
tomography (SPECT) cannot sensitively detect micro cancers. If micro cancers can be
detected, a primary cancer can be cured by operation or radiotherapy or even a metastatic
cancer is curable for a life-sustaining way by early pharmaceutical intervention. Next, there
are the needs for the differentiation between a cancer lesion and a benign lesion. The
current diagnostic modalities often misdiagnose a benign lesion as a cancer lesion. If
differentiation can be made between a cancer lesion and a benign lesion, unnecessary biopsy
can be decreased. Furthermore, there are the needs for the intraoperative visualization of
cancer lesion. At present, the position or extent of a cancer lesion cannot be accurately
determined during the operation of cancers including breast cancer, bladder cancer, and skin
cancer. Therefore, the cancer lesion cannot be completely resected, and there is a risk of
ending the operation while leaving the cancer cells. Moreover, there are the needs for the
correct determination of the positions of cancer lesion. Even if postoperative recurrence and
metastasis are suspected due to the elevation of a tumor marker in blood, the current
diagnostic modalities cannot visualize a metastatic micro cancer. Therefore, the optimum
treatment cannot be selected because whether or not the cancer has actually metastasized or
which organ the cancer has metastasized to cannot be determined. Thus, it is also useful to visualize cancer lesion by molecular imaging techniques such as fluorescent imaging and y ray imaging (PET and SPECT) using an antibody specifically binding to human cancer specific MUC1 as an in vivo diagnostic drug. However, any previous case using an anti human cancer-specific MUC1 antibody as an in vivo diagnostic drug has not been known.
[0006] There is the further needs for a cancer therapeutic drug such as drug conjugated an
antibody. The antibody drug is expected as a method for treating a cancer with fewer
adverse reactions because of specific delivery to a cancer lesion. Radioimmunotherapy
using an antibody bound to a radioisotope (Takashi Tsuruo, "Molecular Target Therapy of
Cancer", NANZANDO Co., Ltd., published on Sep. 15, 2008, p. 332-336; J. Nucl. Med.,
2016 Jul; 57 (7): 1105-1111; and Nucl. Med. Biol., 2010 Nov; 37 (8): 949-955),
photoimmunotherapy using an antibody bound to IRDye700DX (Nat. Med., 2011 Dec; 17
(12): 1685-91), and the like have been reported. IRDye700DX is a near-infrared fluorescent
dye that can also be used in diagnosis. It has been reported that cell death can be induced in
a cancer-specific manner through the phototoxic effect of IRDye700DX by binding this to an
antibody against an antigen expressed on a cancer cell membrane, and allowing the resultant
to specifically accumulate in cancer tissues, followed by irradiation with near-infrared light
(Nat. Med., 2011 Dec; 17 (12): 1685-91). However, any previous case of clinically
applying an antibody drug of an anti-human cancer-specific MUC Iantibody bound to a
cancer therapeutic drug has not been known.
[0007] In general, antibodies have a long half-life in blood and require a period as long as 4
days to 5 days for reaching a tumor-to-blood ratio that confers a signal-to-background ratio
sufficient for visualizing a cancer, after administration into the body (Clin. Pharmacol. Ther.,
2010May;87(5):586-92). Also, the Fe regions of antibodies cause apharmacological
effect such as antibody-dependent cellular cytotoxicity (ADCC) or complement-dependent
cytotoxicity (CDC) (NPL 1; and Curr. Opin. Biotechnol., 2002 Dec; 13 (6): 609-14).
Furthermore, antibodies highly accumulate in the liver regardless of a target, and cancer cells
such as breast cancer are highly to metastasize to the liver. The accumulation in the liver
interfere with the detection of hepatic metastasis at the time of diagnosis of systemic cancer lesion (Clin. Pharmacol. Ther., 2010 May; 87 (5): 586-92).
[0008] For example, low-molecular recombinant antibody fragments such as Fab, scFv,
diabody, and minibody are expected to be utilized as therapeutic antibodies because of easy
reaching to foci with their high tissue penetration and low cost production by using an
expression system in E. coli or yeast. And also, they are reported to be utilized as
diagnostic drug because of their short half-lives in blood and the feature of renal excretion
(Nat. Biotechnol., 2005 Sep; 23 (9): 1126-36).
CITATION LIST PATENT LITERATURE
[0009] PTL 1: W02010/050528
PTL 2: W02008/040362
NON PATENT LITERATURE
[0010] NPL 1: Glycoconj. J., 2013 Apr; 30 (3): 227-36
NPL 2: Cancer Immunol Immunother, 2006 Nov; 55 (11): 1337-47
SUMMARY OF INVENTION TECHNICAL PROBLEM
[0011] Monovalent Fab fragments have a molecular weight of approximately 50 kDa,
which is smaller than antibodies which have a molecular weight of approximately 150 kDa,
are eliminated by renal excretion, and also have a short half-life in blood. Hence, they reach
a tumor-to-blood ratio that confers a signal-to-background ratio sufficient for visualizing a
cancer, within 2 to 32 hours after administration. They lack an Fc region and therefore
cause neither ADCC nor CDC. The Fab fragments are typically eliminated by renal
excretion and therefore, do not interfere with the detection of hepatic metastasis. From
these features, the Fab fragments can be expected to be more effective as in vivo diagnostic
drugs as compared with antibodies.
[0012] However, the binding activity of the Fab fragments is often attenuated because of
being monovalent, not divalent. Antibodies must be labeled with a detectable substance
such as a fluorescent dye or a contrast medium for their utilization as in vivo diagnostic drugs or drugs for use in photoimmunotherapy methods. A further problem is the attenuation of their binding activity due to labeling with such a substance.
[0013] An object of the present invention is to provide an anti-human MUCI antibody Fab fragment that has excellent binding activity and is expected to accumulate in a cancer focus
within a given time (e.g., 24 hours) after administration. Another object of the present
invention is to provide a composition for diagnosis comprising the Fab fragment and a
diagnosis method using the same, and to provide a composition for treatment comprising the Fab fragment and a treatment method using the same.
SOLUTION TO PROBLEM
[0014] The present inventors have conducted considerable diligent studies on the preparation of an anti-human MUC Iantibody Fab fragment having excellent binding activity
against human cancer-specific MUC1, and consequently prepared an anti-human MUC
antibody Fab fragment comprising a heavy chain variable region consisting of the amino acid
sequence represented by SEQ ID NO: 8 or SEQ ID NO: 10, and a light chain variable region consisting of the amino acid sequence represented by SEQ ID NO: 12 (Example 1) and found
that: the anti-human MUC1 antibody Fab fragment has excellent binding activity against
human cancer-specific MUC1 (Example 3) and is free from the attenuation of the binding
activity against human cancer-specific MUC1 by fluorescent labeling and labeling with a
chelating agent (Example 5 and Example 7); and a conjugate comprising the anti-human
MUC Iantibody Fab fragment is useful in the diagnosis of cancers (Example 8, Example 12
and Example 13) and exhibits an antitumor effect in subcutaneously cancer-bearing models
(Example 15).
[0015] Asa result, a diagnosis approach and a treatment approach using the anti-human
MUC1 antibody Fab fragment and the conjugate comprising the anti-human MUC1 antibody
Fab fragment are provided.
[0016] The present invention includes aspects given below as medically or industrially
useful substances and methods.
[0017] Specifically, in one aspect, the present invention can be as follows:
[1] An anti-human MUC Iantibody Fab fragment selected from the group consisting of the following (a) and (b):
(a) an anti-human MUC1 antibody Fab fragment comprising a heavy chain fragment
comprising a heavy chain variable region consisting of the amino acid sequence represented
by SEQ ID NO: 8 or SEQ ID NO: 10 and a light chain comprising a light chain variable
region consisting of the amino acid sequence represented by SEQ ID NO: 12; and
(b) an anti-human MUC1 antibody Fab fragment comprising a heavy chain fragment
comprising a heavy chain variable region derived from a heavy chain variable region
consisting of the amino acid sequence represented by SEQ ID NO: 8 or SEQ ID NO: 10 by
the modification of glutamine at amino acid position 1 of SEQ ID NO: 8 or SEQ ID NO: 10
into pyroglutamic acid, and a light chain comprising a light chain variable region consisting
of the amino acid sequence represented by SEQ ID NO: 12.
[2] The anti-human MUC1 antibody Fab fragment according to [1] which is selected
from the group consisting of the following (a) and (b):
(a) an anti-human MUC Iantibody Fab fragment comprising a heavy chain fragment
consisting of the amino acid sequence represented by SEQ ID NO: 2 or SEQ ID NO: 4 and a
light chain consisting of the amino acid sequence represented by SEQ ID NO: 6; and
(b) an anti-human MUC antibody Fab fragment comprising a heavy chain fragment derived
from a heavy chain fragment consisting of the amino acid sequence represented by SEQ ID
NO: 2 or SEQ ID NO: 4 by the modification of glutamine at amino acid position 1 of SEQ ID
NO: 2 or SEQ ID NO: 4 into pyroglutamic acid, and a light chain consisting of the amino
acid sequence represented by SEQ ID NO: 6.
[3] The anti-human MUCl antibody Fab fragment according to [1] which is selected
from the group consisting of the following (a) and (b):
(a) an anti-human MUC1 antibody Fab fragment comprising a heavy chain fragment
comprising a heavy chain variable region consisting of the amino acid sequence represented
by SEQ ID NO: 10 and a light chain comprising a light chain variable region consisting of
the amino acid sequence represented by SEQ ID NO: 12; and
(b) an anti-human MUC Iantibody Fab fragment comprising a heavy chain fragment comprising a heavy chain variable region derived from a heavy chain variable region
consisting of the amino acid sequence represented by SEQ ID NO: 10 by the modification of glutamine at amino acid position 1 of SEQ ID NO: 10 into pyroglutamic acid, and a light
chain comprising a light chain variable region consisting of the amino acid sequence
represented by SEQ ID NO: 12.
[4] The anti-human MUC Iantibody Fab fragment according to [3] which is selected
from the group consisting of the following (a) and (b):
(a) an anti-human MUC Iantibody Fab fragment comprising a heavy chain fragment
consisting of the amino acid sequence represented by SEQ ID NO: 4 and a light chain consisting of the amino acid sequence represented by SEQ ID NO: 6; and
(b) an anti-human MUC1 antibody Fab fragment comprising a heavy chain fragment derived from a heavy chain fragment consisting of the amino acid sequence represented by SEQ ID
NO: 4 by the modification of glutamine at amino acid position 1 of SEQ ID NO: 4 into
pyroglutamic acid, and a light chain consisting of the amino acid sequence represented by
SEQ ID NO: 6.
[5] The anti-human MUC Iantibody Fab fragment according to [4] which is an anti
human MUC1 antibody Fab fragment comprising a heavy chain fragment consisting of the
amino acid sequence represented by SEQ ID NO: 4 and a light chain consisting of the amino
acid sequence represented by SEQ ID NO: 6.
[6] The anti-human MUC Iantibody Fab fragment according to [4] which is an anti human MUC1 antibody Fab fragment comprising a heavy chain fragment derived from a
heavy chain fragment consisting of the amino acid sequence represented by SEQ ID NO: 4
by the modification of glutamine at amino acid position 1 of SEQ ID NO: 4 into
pyroglutamic acid, and a light chain consisting of the amino acid sequence represented by
SEQ ID NO: 6.
[7] A conjugate comprising one or more labeling moiety and the anti-human MUCI
antibody Fab fragment according to any of [1] to [6].
[8] The conjugate according to [7], wherein the labeling moiety is (i) a ligand and a linker, (ii) a ligand, (iii) a fluorescent dye and a linker, or (iv) a fluorescent dye.
[9] The conjugate according to [8], wherein the labeling moiety is (i) a ligand and a linker or (ii) a ligand.
[10] The conjugate according to [9], wherein the ligand is a ligand represented by the following formula (A):
[0018] [Chemical Formula 1]
NH
0H H
00 OHH H 3C. 04
H H
wherein the wavy line represents binding to the anti-human MUC1 antibody Fab fragment or
the linker.
[11] The conjugate according to [10], wherein the labeling moiety is a ligand and a linker
represented by the following formula (A'):
[0019] [Chemical Formula2]
0
OH NH N
0
N-OH (A') 0 NH H3 C_ O H
N N N S H H OH wherein the wavy line represents binding to the anti-human MUC1 antibody Fab fragment.
[12] The conjugate according to [11], wherein the anti-human MUC1 antibody Fab
fragment is bound via an amino group thereof to the carbon atom of a labeling moiety terminal C(=S) group.
[13] A conjugate selected from the group consisting of the following (a) to (c):
(a) the conjugate according to [12] wherein the anti-human MUC1 antibody Fab fragment is
the anti-human MUC1 antibody Fab fragment according to [5];
(b) the conjugate according to [12] wherein the anti-human MUC1 antibody Fab fragment is
the anti-human MUC1 antibody Fab fragment according to [6]; and
(c) a conjugate which is a mixture of (a) and (b).
[14] The conjugate according to any of [9] to [13], further comprising a metal.
[15] The conjugate according to [14], wherein the metal is a metal radioisotope.
[16] The conjugate according to [15], wherein the metal is 89Zr.
[17] The conjugate according to [13], further comprising 89Zr.
[18] The conjugate according to [8], wherein the labeling moiety is (i) a fluorescent dye
and a linker or (ii) a fluorescent dye.
[19] The conjugate according to [18], wherein the fluorescent dye is a fluorescent dye selected from the group consisting of the following formula (B) and the following formula
(C):
[0020] [Chemical Formula 3] SO 3 Na
NaO,3S SO3~
N N*
SO 3Na
(B)
[0021] [Chemical Formula4] SO 3Na
O N' SO3'
N N -N SO 3 Na
SO3Na N N N
O NS
SO 3Na
(C) wherein the wavy line represents binding to the anti-human MUC1 antibody Fab fragment or the linker.
[20] The conjugate according to [19], wherein the wavy line represents binding to the anti-human MUC1 antibody Fab fragment, and the anti-human MUC antibody Fab fragment
is bound via an amino group thereof to the carbon atom of a labeling moiety terminal C(=O)
group.
[21] The conjugate according to [20], wherein the labeling moiety is a fluorescent dye represented by formula (B).
[22] A conjugate selected from the group consisting of the following (a) to (c): (a) the conjugate according to [21] wherein the anti-human MUC1 antibody Fab fragment is
the anti-human MUCI antibody Fab fragment according to [5]; (b) the conjugate according to [21] wherein the anti-human MUC1 antibody Fab fragment is
the anti-human MUC Iantibody Fab fragment according to [6]; and
(c) a conjugate which is a mixture of (a) and (b).
[23] The conjugate according to [20], wherein the labeling moiety is a fluorescent dye
represented by formula (C).
[24] A conjugate selected from the group consisting of the following (a) to (c):
(a) the conjugate according to [23] wherein the anti-human MUC1 antibody Fab fragment is
the anti-human MUC Iantibody Fab fragment according to [5];
(b) the conjugate according to [23] wherein the anti-human MUCl antibody Fab fragment is
the anti-human MUC1 antibody Fab fragment according to [6]; and
(c) a conjugate which is a mixture of (a) and (b).
[25] A polynucleotide selected from the group consisting of the following (a) and (b):
(a) a polynucleotide comprising a nucleotide sequence encoding the heavy chain fragment of
the anti-human MUC1 antibody Fab fragment according to [1]; and
(b) a polynucleotide comprising a nucleotide sequence encoding the light chain of the anti
human MUC Iantibody Fab fragment according to [1].
[26] A polynucleotide selected from the group consisting of the following (a) and (b): (a) a polynucleotide comprising a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC Iantibody Fab fragment according to [5]; and (b) a polynucleotide comprising a nucleotide sequence encoding the light chain of the anti human MUC1 antibody Fab fragment according to [5].
[27] An expression vector comprising the following (a) and/or (b):
(a) a polynucleotide comprising a nucleotide sequence encoding the heavy chain fragment of
the anti-human MUC Iantibody Fab fragment according to [1]; and
(b) a polynucleotide comprising a nucleotide sequence encoding the light chain of the anti
human MUC1 antibody Fab fragment according to [1].
[28] An expression vector comprising the following (a) and/or (b): (a) a polynucleotide comprising a nucleotide sequence encoding the heavy chain fragment of
the anti-human MUC1 antibody Fab fragment according to [5]; and
(b) a polynucleotide comprising a nucleotide sequence encoding the light chain of the anti
human MUC Iantibody Fab fragment according to [5].
[29] A host cell selected from the group consisting of the following (a) to (d):
(a) a host cell transformed with an expression vector comprising a polynucleotide comprising
a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC Iantibody
Fab fragment according to [1]; (b) a host cell transformed with an expression vector comprising a polynucleotide comprising
a nucleotide sequence encoding the light chain of the anti-human MUC1 antibody Fab
fragment according to [1];
(c) a host cell transformed with an expression vector comprising a polynucleotide comprising
a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC Iantibody
Fab fragment according to [1] and a polynucleotide comprising a nucleotide sequence
encoding the light chain of the anti-human MUC1 antibody Fab fragment according to [1];
and
(d) a host cell transformed with an expression vector comprising a polynucleotide comprising
a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC1 antibody
Fab fragment according to [1] and an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding the light chain of the anti-human MUC Iantibody
Fab fragment according to [1].
[30] A host cell selected from the group consisting of the following (a) to (d): (a) a host cell transformed with an expression vector comprising a polynucleotide comprising
a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC1 antibody
Fab fragment according to [5]; (b) a host cell transformed with an expression vector comprising a polynucleotide comprising
a nucleotide sequence encoding the light chain of the anti-human MUC Iantibody Fab
fragment according to [5];
(c) a host cell transformed with an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC1 antibody
Fab fragment according to [5] and a polynucleotide comprising a nucleotide sequence
encoding the light chain of the anti-human MUC1 antibody Fab fragment according to [5];
and (d) a host cell transformed with an expression vector comprising a polynucleotide comprising
a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC1 antibody
Fab fragment according to [5] and an expression vector comprising a polynucleotide
comprising a nucleotide sequence encoding the light chain of the anti-human MUC Iantibody
Fab fragment according to [5].
[31] A method for producing an anti-human MUC1 antibody Fab fragment comprising
the step of culturing a host cell selected from the group consisting of the following (a) to (c)
to express the anti-human MUC Iantibody Fab fragment:
(a) a host cell transformed with an expression vector comprising a polynucleotide comprising
a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC Iantibody
Fab fragment according to [1] and a polynucleotide comprising a nucleotide sequence
encoding the light chain of the anti-human MUC1 antibody Fab fragment according to [1];
(b) a host cell transformed with an expression vector comprising a polynucleotide comprising
a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC1 antibody
Fab fragment according to [1] and an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding the light chain of the anti-human MUCi antibody
Fab fragment according to [1]; and
(c) a host cell transformed with an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC1 antibody
Fab fragment according to [1], and a host cell transformed with an expression vector
comprising a polynucleotide comprising a nucleotide sequence encoding the light chain of
the anti-human MUC1 antibody Fab fragment according to [1].
[32] A method for producing an anti-human MUC1 antibody Fab fragment comprising the step of culturing a host cell selected from the group consisting of the following (a) to (c)
to express the anti-human MUC Iantibody Fab fragment:
(a) a host cell transformed with an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC Iantibody
Fab fragment according to [5] and a polynucleotide comprising a nucleotide sequence
encoding the light chain of the anti-human MUC1 antibody Fab fragment according to [5];
(b) a host cell transformed with an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC1 antibody
Fab fragment according to [5] and an expression vector comprising a polynucleotide
comprising a nucleotide sequence encoding the light chain of the anti-human MUC1 antibody
Fab fragment according to [5]; and
(c) a host cell transformed with an expression vector comprising a polynucleotide comprising
a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC1 antibody
Fab fragment according to [5], and a host cell transformed with an expression vector
comprising a polynucleotide comprising a nucleotide sequence encoding the light chain of
the anti-human MUC1 antibody Fab fragment according to [5].
[33] A method for producing a conjugate comprising a labeling moiety and an anti
human MUC1 antibody Fab fragment, comprising the steps of: producing the anti-human
MUC antibody Fab fragment by the method according to [31] or [32]; and covalently binding the Fab fragment to the labeling moiety.
[34] The method for producing a conjugate according to [33], wherein the step of
covalently binding the Fab fragment to the labeling moiety is the step of i) binding the Fab
fragment via a linker to a ligand or ii) covalently binding the Fab fragment directly to a ligand.
[35] The method for producing a conjugate according to [34], further comprising the step of labeling the ligand of the conjugate with a metal radioisotope.
[36] The method for producing a conjugate according to [33], wherein the step of
covalently binding the Fab fragment to the labeling moiety is the step of i) binding the Fab
fragment via a linker to a fluorescent dye or ii) covalently binding the Fab fragment directly to a fluorescent dye.
[37] A composition for diagnosis comprising one or more conjugate according to any of
[7] to [24], and a pharmaceutically acceptable carrier.
[38] The composition for diagnosis according to [37], wherein the conjugate is the
conjugate according to any of [17], [22] and [24].
[39] The composition for diagnosis according to [38], wherein the conjugate is the
conjugate according to [17].
[40] The composition for diagnosis according to [38], wherein the conjugate is the
conjugate according to [22].
[41] The composition for diagnosis according to [38], wherein the conjugate is the
conjugate according to [24].
[42] The composition for diagnosis according to any of [37] to [41] which is used in the
diagnosis of a cancer expressing human MUC1.
[43] The composition for diagnosis according to [42], wherein the cancer is breast cancer
or bladder cancer.
[44] A pharmaceutical composition comprising one or more conjugate according to any
of [7] to [24], and a pharmaceutically acceptable carrier.
[45] The pharmaceutical composition according to [44], wherein the conjugate is the conjugate according to any of [17], [22] and [24].
[46] The pharmaceutical composition according to [45], wherein the conjugate is the
conjugate according to [24].
[47] The pharmaceutical composition according to any of [44] to [46] which is a
pharmaceutical composition for treating a cancer expressing human MUC1.
[48] The pharmaceutical composition according to [47], wherein the cancer is breast cancer or bladder cancer.
[49] Use of the conjugate according to any of [7] to [24] for the production of a composition for the diagnosis of breast cancer or bladder cancer and/or a pharmaceutical
composition for treating breast cancer or bladder cancer.
[50] The conjugate according to any of [7] to [24] for use in the diagnosis and/or
treatment of breast cancer or bladder cancer.
[51] A method for diagnosing breast cancer or bladder cancer, comprising preoperatively
or intraoperatively administering the conjugate according to any of [7] to [24] to a subject.
[52] A method for treating breast cancer or bladder cancer, comprising the step of
administering a therapeutically effective amount of the conjugate according to any of [7] to
[24]. ADVANTAGEOUS EFFECTS OF INVENTION
[0022] The anti-human MUC1 antibody Fab fragment of the present invention has excellent
binding activity against human cancer-specific MUC1 and is expected to be useful in the diagnosis and/or treatment of cancers such as breast cancer.
BRIEF DESCRIPTION OF DRAWINGS
[0023] Fig. 1 is a graph and a table showing the binding activity of P10-1 Fab, P10-2 Fab
and 1B2 Fab of Comparative Example against human cancer-specific MUC.
Fig. 2 is a graph and a table showing the binding activity of P10-1 Fab Dye, P10-2
Fab Dye and 1B2 Fab Dye of Comparative Example against human cancer-specific MUC1.
Fig. 3 is a graph and a table showing the binding activity of P10-2 Fab DFO and P10-2 Fab against human cancer-specific MUC1.
Fig. 4 is a graph showing the binding activity of P10-2 Fab against breast cancer cell
line MDA-MB-468 cells (also referred to as MM-468 cells) and bladder cancer cell line 647
V cells expressing human cancer-specific MUC1. The horizontal axis depicts the
concentration (Log(mg/mL)) of P10-2 Fab, and the vertical axis depicts luminescence.
Fig. 5A is representative photographs taken with a usual camera (left) and a near
infrared fluorescence camera (center and right) 6 hours after administration of P10-2 Fab Dye
which was intravenously administered at 3 mg/kg to subcutaneously cancer-bearing models.
Fig. 5B is a graph quantifying the tumor/background ratio of a tumor site and a
peritumoral background site and indicates mean + standard error. The horizontal axis
depicts the dose and time after administration of P10-2 Fab Dye.
Fig. 6 is a graph quantifying luminescence of the tumor sites of administering P10-2
Fab IR700 to MM-468 cell-transplanted mice, euthanizing the animals 2 hours after the
administration, excising tumor, taking photographs with IVIS SPECTRUM. The vertical
axis depicts luminescence.
Fig. 7 is a graph showing results of measuring cytotoxicity of reacting P10-2 Fab
IR700 to MM-468 cells, 647-V cells or CHO-Kl cells with irradiating light of Comparative
Example. The upper column of the horizontal axis of each graph depicts the concentration
of P10-2 Fab IR700, and the lower column depicts the exposure of light. The vertical axis
depicts luminescence and indicates mean + standard error.
Fig. 8 is a graph showing results of measuring an antitumor effect depending on the
presence or absence of light irradiation (0 J or 200 J) at the time of P10-2 Fab IR700
administration using MM-468 cell-transplanted nude mice. The horizontal axis depicts the
number of days when the day on which tumor volume became 300 mm3 was defined as day
1. The vertical axis depicts tumor volume (mm3 ) and indicates mean + standard error.
DESCRIPTION OF EMBODIMENTS
[0024] Hereinafter, the present invention will be described in detail. However, the present
invention is not limited thereby. Scientific terms and technical terms used in relation to the
present invention have meanings generally understood by those skilled in the art, unless otherwise specified herein.
[0025] The present inventors have conducted considerable diligent studies on the
preparation of an anti-human cancer-specific MUC1 antibody or an antigen binding fragment
thereof and consequently successfully prepared an anti-human MUC1 antibody Fab fragment having the ability to strongly bind to cancer-specific MUC1.
[0026] The basic structure of an antibody molecule is common among classes and is
constituted by heavy chains having a molecular weight of 50000 to 70000 and light chains having a molecular weight of 20000 to 30000. The heavy chain usually consists of a
polypeptide chain comprising approximately 440 amino acids, has a structure characteristic
of each class, and is called y, p, u, S, and 6 chains corresponding to IgG, IgM, IgA, IgD, and
IgE. IgG further has IgG1, IgG2, IgG3, and IgG4 which are called yl, y2,y3, and 74, respectively. The light chain usually consists of a polypeptide chain comprising
approximately 220 amino acids and known as two types, L and K types, which are called
and K chains, respectively. As for the peptide configuration of the basic structure of the
antibody molecule, two homologous heavy chains and two homologous light chains are linked through disulfide bonds (S-S bonds) and non-covalent bonds to form a molecular
weight of 150000 to 190000. The two light chains can pair with any of the heavy chains. An individual antibody molecule is constantly made up of two identical light chains and two
identical heavy chains.
[0027] Four (or five for and c chains) and two intrachain S-S bonds are present in the
heavy chain and the light chain, respectively, and each constitute one loop per 100 to 110 amino acid residues. This conformation is similar among the loops and is called structural
unit or domain. For both the heavy chain and the light chain, a domain positioned at the N
terminus does not have a constant amino acid sequence even among preparations from the
same classes (subclasses) of animals of the same species, and is thus called variable region.
The respective domains are called heavy chain variable region (VH domain) and light chain
variable region (VL domain). An amino acid sequence on the C-terminal side therefrom is
almost constant on a class or subclass basis and called constant region. The respective domains are represented by CH1, CH2, CH3 and CL.
[0028] The binding specificity of the antibody for an antigen depends on the amino acid
sequence of a moiety constituted by the heavy chain variable region and the light chain
variable region. On the other hand, biological activity such as binding to complements or various cells reflects the difference in structure among the constant regions of Igs of respective classes. It is known that the variability of the heavy chain and light chain
variable regions is limited substantially by three small hypervariable regions present in both
the chains. These regions are called complementarity determining regions (CDRs; CDR1, CDR2, and CDR3 in order from the N-terminal side). The remaining moieties of the
variable region are called framework regions (FRs) and are relatively constant.
[0029] A region between the CH1 domain and the CH2 domain of the heavy chain constant region of an antibody is called hinge region. This region is rich in proline residues and contains a plurality of interchain S-S bonds that connect two heavy chains. For example, the hinge regions of human IgG1, IgG2, IgG3, and IgG4 contain 2, 4, 11, and 2 cysteine
residues, respectively, which constitute S-S bonds between the heavy chains. The hinge
region is a region highly sensitive to a proteolytic enzyme such as papain or pepsin. In the case of digesting an antibody with papain, the heavy chains are cleaved at a position on the
N-terminal side from the inter-heavy chain S-S bonds of the hinge region and thus
decomposed into two Fab fragments and one Fc fragment. The Fab fragment is constituted by a light chain and a heavy chain fragment comprising a heavy chain variable region (VH),
a CH1 domain and a portion of the hinge region. The Fab fragment comprises variable
regions and has antigen binding activity.
[0030] <Anti-human MUCI antibody Fab fragment of present invention>
The anti-human MUC1 antibody Fab fragment of the present invention is a Fab fragment having the following feature:
an anti-human MUC1 antibody Fab fragment comprising a heavy chain fragment
comprising a heavy chain variable region consisting of the amino acid sequence represented
by SEQ ID NO: 8 or SEQ ID NO: 10 and a light chain comprising a light chain variable region consisting of the amino acid sequence represented by SEQ ID NO: 12.
[0031] In one embodiment, the anti-human MUC1 antibody Fab fragment of the present invention is an anti-human MUC1 antibody Fab fragment comprising a heavy chain fragment
comprising a heavy chain variable region consisting of the amino acid sequence represented
by SEQ ID NO: 10 and a light chain comprising a light chain variable region consisting of the amino acid sequence represented by SEQ ID NO: 12.
[0032] Any constant region of Igyl, Igy2, Igy3 or Igy4, etc. can be selectable as the heavy chain constant region of the anti-human MUC Iantibody Fab fragment of the present
invention. In one embodiment, the heavy chain constant region of the anti-human MUC1 antibody Fab fragment of the present invention is a human Igyl constant region.
[0033] Any constant region of Igk or IgK can be selectable as the light chain constant region of the anti-human MUC1 antibody Fab fragment of the present invention. Inone embodiment, the light chain constant region of the anti-human MUC1 antibody Fab fragment of the present invention is a human IgK constant region.
[0034] In one embodiment, the anti-human MUC1 antibody Fab fragment of the present
invention is the following Fab fragment:
an anti-human MUC1 antibody Fab fragment comprising a heavy chain fragment
consisting of the amino acid sequence represented by SEQ ID NO: 2 or SEQ ID NO: 4 and a
light chain consisting of the amino acid sequence represented by SEQ ID NO: 6.
[0035] In one embodiment, the anti-humanMUCI antibody Fab fragment of the present
invention is an anti-human MUC1 antibody Fab fragment comprising a heavy chain fragment
consisting of the amino acid sequence represented by SEQ ID NO: 4 and a light chain consisting of the amino acid sequence represented by SEQ ID NO: 6.
[0036] In the case of expressing an antibody including a Fab fragment in cells, the antibody
is known to undergo a posttranslational modification. Examples of the posttranslational
modification include the cleavage of heavy chain C-terminal lysine by carboxypeptidase, the
modification of heavy chain and light chain N-terminal glutamine or glutamic acid into
pyroglutamic acid by pyroglutamylation, glycosylation, oxidation, deamidation, and glycation. Such a posttranslational modification is known to occur in various antibodies (J.
Pharm. Sci., 2008; 97: 2426-2447).
[0037] The anti-human MUC1 antibody Fab fragment of the present invention can also
include a Fab fragment resulting from the posttranslational modification. Examples of the
anti-human MUC1 antibody Fab fragment of the present invention resulting from the
posttranslational modification include an anti-human MUC Iantibody Fab fragment having
an N-terminally pyroglutamylated heavy chain. It is known in the art that such a
posttranslational modification by N-terminal pyroglutamylation has no influence on the
activity of the antibody (Anal. Biochem., 2006; 348: 24-39).
[0038] In one embodiment, the anti-human MUCI antibody Fab fragment of the present
invention is an anti-human MUCl antibody Fab fragment having the following feature:
an anti-human MUC Iantibody Fab fragment comprising a heavy chain fragment
comprising a heavy chain variable region derived from a heavy chain variable region
consisting of the amino acid sequence represented by SEQ ID NO: 8 or SEQ ID NO: 10 by
the modification of glutamine at amino acid position 1 of SEQ ID NO: 8 or SEQ ID NO: 10
into pyroglutamic acid, and a light chain comprising a light chain variable region consisting
of the amino acid sequence represented by SEQ ID NO: 12.
[0039] Ina certain embodiment, the anti-human MUCI antibody Fab fragment of the
present invention is an anti-human MUC Iantibody Fab fragment having the following
feature:
an anti-human MUC1 antibody Fab fragment comprising a heavy chain fragment
comprising a heavy chain variable region derived from a heavy chain variable region
consisting of the amino acid sequence represented by SEQ ID NO: 10 by the modification of
glutamine at amino acid position 1 of SEQ ID NO: 10 into pyroglutamic acid, and a light
chain comprising a light chain variable region consisting of the amino acid sequence
represented by SEQ ID NO: 12.
[0040] In an alternative embodiment, the anti-MUC1 antibody Fab fragment of the present
invention is an anti-human MUC Iantibody Fab fragment having the following feature: an anti-human MUC1 antibody Fab fragment comprising a heavy chain fragment derived from a heavy chain fragment consisting of the amino acid sequence represented by
SEQ ID NO: 2 or SEQ ID NO: 4 by the modification of glutamine at amino acid position 1 of
SEQ ID NO: 2 or SEQ ID NO: 4 into pyroglutamic acid, and a light chain consisting of the
amino acid sequence represented by SEQ ID NO: 6.
[0041] Ina certain embodiment, the anti-MUC1 antibody Fab fragment of the present
invention is an anti-human MUC Iantibody Fab fragment having the following feature:
an anti-human MUC1 antibody Fab fragment comprising a heavy chain fragment
derived from a heavy chain fragment consisting of the amino acid sequence represented by
SEQ ID NO: 4 by the modification of glutamine at amino acid position 1 of SEQ ID NO: 4
into pyroglutamic acid, and a light chain consisting of the amino acid sequence represented
by SEQ ID NO: 6.
[0042] The anti-human MUC1 antibody Fab fragment of the present invention binds to
human cancer-specific MUC1. The cancer-specific MUC1 is expressed in cancers such as
breast cancer, lung cancer, colorectal cancer, bladder cancer, skin cancer, thyroid gland
cancer, stomach cancer, pancreatic cancer, kidney cancer, ovary cancer or uterine cervical
cancer. A method for measuring the binding activity of the obtained anti-human MUC1
antibody Fab fragment against human cancer-specific MUC1 includes methods such as
ELISA and FACS. In the case of using, for example, ELISA, human cancer-specific
MUCI-positive cells (e.g., T-47D cells) are immobilized onto an ELISA plate, to which the
Fab fragment is then added and reacted, and then, an anti-IgK antibody or the like labeled
with horseradish peroxidase or the like is reacted. Then, the binding of the secondary
antibody is identified by activity measurement using a reagent for detecting the activity
thereof (e.g., a chemiluminescent horseradish peroxidase substrate for the horseradish
peroxidase label) or the like.
[0043] The anti-human MUCI antibody Fab fragment of the present invention can be
readily prepared by those skilled in the art using a method known in the art on the basis of
sequence information on the heavy chain fragment and the light chain of the anti-human
MUCI antibody Fab fragment of the present invention disclosed herein. Theanti-human
MUC Iantibody Fab fragment of the present invention can be produced according to, but not
particularly limited to, a method described in, for example, <Method for producing anti
human MUC1 antibody Fab fragment according to present invention> mentioned later.
[0044] <Conjugate of present invention>
The conjugate of the present invention is a conjugate comprising a labeling moiety
and the anti-human MUC1 antibody Fab fragment of the present invention.
[0045] The "labeling moiety" is (i) a ligand and a linker, (ii) a ligand, (iii) a fluorescent dye
and a linker, or (iv) a fluorescent dye. A certain embodiment is (i) a ligand and a linker, or
(ii) a ligand. A certain embodiment is (i) a fluorescent dye and a linker, or (ii) a fluorescent
dye. The ligand of the "labeling moiety" may further comprise a metal. A certain
embodiment is (i) a ligand and a linker or (ii) a ligand comprising a metal, and in other
words, is (i) a ligand that has formed a chelate complex with a metal, and a linker, or (ii) a
ligand that has formed a chelate complex with a metal.
[0046] The conjugate of the present invention comprising a metal or a fluorescent dye can
be used in various contrast media and/or cancer therapeutic agents and is used in, for
example, an MRI contrast medium, a PET tracer, a fluorescently labeled molecular imaging
agent, and a drug for use in photoimmunotherapy methods.
[0047] In the present specification, the "metal" means a paramagnetic metal ion or a metal
radioisotope.
[0048] The paramagnetic metal ion is suitably used in an MRI contrast medium.
Examples of the embodiment of the paramagnetic metal ion include, but are not limited to, 3+, D>, Fe2+, Fe 3+, Cu2 +, Ni 2+, Rh2+, C02+,Gd3+, Eu Tb3+, Pm3+, Nd, Tm3+, Ce>*, Y3 *, Ho>3,
Er3+, La+, Yb3+, Mn+, and Mn2. A certain embodiment is Gd3+, Mn3, Mn2+, Fe2+, or Fe3+.
A certain embodiment is Mn3+ or Mn 2+. In this case, halogen or the like can be used as a
counter anion in the conjugate. Alternatively, the counter anion may be C(=O)O~ of the
ligand. The conjugate may further have a counter cation such as Na*.
[0049] The metal radioisotope is used in, for example, a PET tracer. Examples of a certain embodiment include, but are not limited to, 89Zr, 51Mn, 2 Fe, 60 Cu, 67 Ga , 68 Ga, 72 As, 99mTc, and"'In. A certain embodiment is89 Zr, 6Cu, 67 Ga, 68Ga, 99mTc,or 1 1 1n. Acertain embodiment is a radioisotope of zirconium. A certain embodiment is 89Zr.
[0050] The "ligand" is a moiety capable of forming a chelate complex with a metal in the
conjugate and means a group constituted by a chelating agent. The constituted group is a group having a bond by the removal of a proton from the chelating agent.
[0051] The "chelating agent" is a compound that can forma coordinate bond with a metal.
[0052] Examples of the "chelating agent" include siderophore and non-siderophore.
Examples of the siderophore include hydroxamic acid type, catechol type, and mixed ligand type. Examples of the hydroxamic acid-type siderophore include ferrichrome, deferoxamine (DFO) represented by the following formula:
[0053] [Chemical Formula 5]
H2 H0 H H3 0 0 OH
fusarinine C, ornibactin, and rhodotorulic acid. Examples of the catechol-type siderophore include enterobactin, bacillibactin, and vibriobactin. Examples of the mixed ligand-type siderophore include azotobactin, pyoverdine, and yersiniabactin. In the case of the siderophore, DFO can be reacted via its reactive functional group -NH 2 with the linker or the
Fab fragment, and the siderophore other than DFO can also be reacted via its reactive
functional group such as a carboxy group, a hydroxy group, or an amino group with the
linker or the Fab fragment by a method usually used by those skilled in the art.
[0054] Examples of the non-siderophore include DTPA (diethylenetriaminepentaacetic
acid, CAS No: 67-43-6), DTPA-BMA (1,7-bis(methylcarbamoylmethyl)-1,4,7-triazaheptane
1,4,7-triacetic acid, CAS No: 119895-95-3), EOB-DTPA (DTPA bound to an ethoxybenzyl
group, CAS No: 158599-72-5), TTHA (triethylenetetraminehexaacetic acid, CAS No: 869-
52-3), DO3A (1,4,7,10-tetraazacyclododecane-1,4,7-triacetic acid, CAS No: 217973-03-0),
HP-DO3A (10-(2-hydroxypropyl)-1,4,7,10-tetraazacyclododecane-1,4,7-triacetic acid, CAS
No: 120041-08-9), DOTA (1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid, CAS
No: 60239-18-1), and known reactive derivatives thereof.
[0055] Compounds and conjugates described herein also encompass free forms and salts thereof unless otherwise specified. In this context, the "salt thereof' is a salt that can be
formed by the compound or the conjugate that may form an acid-addition salt or a salt with a base depending on the type of a substituent in the compound or the conjugate. Specific examples thereof include: acid-addition salts with inorganic acids such as hydrochloric acid, hydrobromic acid, hydroiodic acid, sulfuric acid, nitric acid, and phosphoric acid, or organic
acids such as formic acid, acetic acid, propionic acid, oxalic acid, malonic acid, succinic acid, fumaric acid, maleic acid, lactic acid, malic acid, mandelic acid, tartaric acid,
dibenzoyltartaric acid, ditoluoyltartaric acid, citric acid, methanesulfonic acid, ethanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic acid, aspartic acid, and glutamic acid; salts with
inorganic bases such as sodium, potassium, magnesium, calcium, and aluminum, or organic
bases such as methylamine, ethylamine, ethanolamine, lysine, and ornithine; salts with various amino acids and amino acid derivatives, such as acetylleucine; and ammonium salts.
For example, DFO exists as deferoxamine methanesulfonate or exists as other salts. DTPA
exits both as a free form and as sodium salt.
[0056] A certain embodiment of the "chelating agent" for use in an MRI contrast medium is
the siderophore or non-siderophore chelating agent described above.
[0057] A certain embodiment of the "chelating agent" for use in a PET tracer is the siderophore or non-siderophore chelating agent described above. A certain embodiment is
MAG3 (mercapto-acetyl-glycine-glycine-glycine, CAS No: 66516-09-4). A certain
embodiment is DFO.
[0058] Examples of a certain embodiment of the "chelating agent" constituting the ligand
contained in the conjugate of the present invention include DFO, DTPA, DTPA-BMA, EOB
DTPA, DO3A, HP-DO3A, and DOTA. A certain embodiment is DFO, DTPA, or DOTA.
A certain embodiment is DFO.
[0059] The "linker is a group that creates a distance between the anti-human MUC1
antibody Fab fragment and the ligand. Examples of a certain embodiment of the "linker" in the conjugate include the following formula:
[0060] [Chemical Formula 6]
g H
H 4
(hereinafter, referred to as -C(=S)-NH-(1,4-phenylene)-NH-C(=S)-), -CH 2-(1,4-phenylene)
NH-C(=S)-, and -C(=O)-(C1 -20 alkylene)-C(=O)-. In this context, the "C1-2o alkylene" is
linear or branched alkylene having 1 to 20 carbon atoms. A certain embodiment of the C1 -20 alkylene is C1 -1 0 alkylene orCi-2alkylene. A certain embodiment of theC1 -20 alkylene is ethylene. A certain embodiment is -C(=S)-NH-(1,4-phenylene)-NH-C(=S)-. A certain
embodiment is -C(=O)-C 2 H 4 -C(=O)-. Examples of a reagent that can be used as the linker
include HO-C(=O)-(C 1 -20 alkylene)-C(=O)-OH, succinic acid, and p-di-NCS-benzene(p
diisocyanobenzene).
[0061] The conjugate of the present invention comprising a fluorescent dye can be used as a
fluorescently labeled molecular imaging agent, a drug for use in photoimmunotherapy
methods, or a fluorescently labeled molecular imaging agent and a drug for use in photoimmunotherapy methods.
[0062] A dye having absorption maximum and emission maximum at a near-infrared
wavelength (650 to 1000 nm) usually used in photoimaging can be used as the fluorescent
dye for use in the conjugate of the present invention. Examples of a certain embodiment of
the fluorescent dye include cyanine and indocyanine compounds. Examples of a certain
embodiment include IRDye800CW and IRDye700DX (LI-COR Bioscience, Inc..), Cy
(Molecular Probes, Inc.), Alexa Fluor, BODIPY, and DyLight (Thermo Fisher Scientific
Inc.), CF790 (Biotium, Inc.), DY (Dyomics GmbH), HiLyte Fluor 680 and HiLyte Fluor 750
(AnaSpec Inc.), and PULSAR650 and QUASAR670 (LGC Biosearch Technologies). A certain embodiment is IRDye800CW represented by the following formula:
[0063] [Chemical Formula 7] SO 3 Na
NaSO 3 ~
/0 N N+
SO3Na NaO2C
or IRDye700DX represented by the following formula:
[0064] [Chemical Formula 8] SO 3 Na
~Nt SO3 COOH SO3 Na
The fluorescent dye can be reacted via its carboxy group, hydroxy group, amino group, or the
like or via an active group introduced by a method usually used by those skilled in the art with the Fab fragment or the linker. A certain embodiment of the fluorescent dye having an introduced active group is a fluorescent dye esterified with a N-hydroxysuccinimide (NHS) group. For example, NHS esters of IRDye800CW and IRDye700DX mentioned above are commercially available, and they can be utilized.
[0065] The binding of the anti-human MUCI antibody Fab fragment of the present
invention to the labeling moiety can be appropriately performed by those skilled in the art
using a known approach. For example, the labeling moiety can be bound to one or more amino groups (e.g., a N-terminal amino group and an amino group of an amino acid side chain), one or more thiol groups (e.g., a thiol group of an amino acid side chain), or one or
more carboxyl groups (e.g., carboxyl groups of the C terminus and an amino acid side chain)
of the anti-human MUC1 antibody Fab fragment of the present invention. Acertain embodiment of the conjugate of the present invention is a conjugate wherein the labeling moiety is bound to one or more amino groups of the anti-human MUCi antibody Fab
fragment of the present invention.
[0066] When the labeling moiety is a ligand and a linker, the conjugate of the present invention may be produced by reacting the chelating agent with a substance obtained through the reaction of the anti-human MUC1 antibody Fab fragment of the present invention with
thelinker. It maybe produced by reacting the anti-human MUC1 antibody Fab fragment of
the present invention with a substance obtained through the reaction of the chelating agent with the linker. As a reaction example, a substance obtained through the reaction of the
amino group of the chelating agent with the linker may be reacted with one or more amino
groups (e.g., an N-terminal amino group and an amino group of a lysine side chain) of the
anti-human MUC1 antibody Fab fragment of the present invention. Reactionof
synthesizing thiourea by adding isothiocyanate to amine, reaction of synthesizing amide by
adding amine and carboxylic acid, or the like can be used in the production of the conjugate.
The reaction can be performed by the application of a method known to those skilled in the
art. A compound of the chelating agent bound to the linker in advance may be used as a
starting material. Examples of the compound of the chelating agent bound to the linker include p-SCN-Bn-DFO (DFO bound to a p-isothiocyanophenylaminothiocarbony group,
CAS No: 1222468-90-7) represented by the following formula:
[0067] [Chemical Formula 9] OH 0 H N HN N
SCNS OH H H3C N
O OH
DTPA bound to a p-isothiocyanobenzyl group (p-NCS-Bn-DTPA, CAS No: 102650-30-6),
DOTA bound to a p-isothiocyanobenzyl group (p-NCS-Bn-DOTA, CAS No: 127985-74-4),
and p-SCN-Bn-CHX-A"-DTPA ([(R)-2-amino-3-(4-isothiocyanatophenyl)propyl]-trans
(S,S)-cyclohexane-1,2-diamine-pentaacetic acid, CAS No: 157380-45-5).
[0068] The metal (paramagnetic metal ion or metal radioisotope) can be added to the anti human MUC1 antibody Fab fragment of the present invention bound to one or more labeling
moiety thus produced by the production method to obtain the conjugate of the present
invention comprising the metal.
[0069] Also, the conjugate of the present invention may be produced as a conjugate which is a Fab fragment bound via an amino group thereof to one or more labeling moiety by
reacting one or more amino groups (e.g., a N-terminal amino group and an amino group of an
amino acid side chain) of the Fab fragment with the labeling moiety having a carboxyl group
or an isothiocyanic acid group activated with N-hydroxysuccinimide (NHS).
[0070] The conjugate of the present invention is a conjugate comprising one or more
labeling moiety and the anti-human MUC1 antibody Fab fragment of the present invention.
A certain embodiment is the anti-human MUC1 antibody Fab fragment bound to 1 to 27
labeling moieties. A certain embodiment is the anti-human MUCI antibody Fab fragment
bound to 1 to 23 labeling moieties. A certain embodiment is the anti-human MUCI antibody Fab fragment bound to 1 to 15 labeling moieties. A certain embodiment is the anti-human MUC1 antibody Fab fragment bound to 1 to 11 labeling moieties. A certain embodiment is the anti-human MUC1 antibody Fab fragment bound to 1 to 9 labeling moieties. A certain embodiment is the anti-human MUC1 antibody Fab fragment bound to 1to 7 labeling moieties. A certain embodiment is the anti-human MUC1 antibody Fab fragment bound to 1to 5 labeling moieties. A certain embodiment is the anti-humanMUC antibody Fab fragment bound to 1 to 4 labeling moieties. A certain embodiment is the anti human MUC antibody Fab fragment bound to one or more labeling moiety further comprising a metal.
[0071] In one embodiment, the conjugate of the present invention is a conjugate wherein
the labeling moiety is (i) a ligand and a linker, (ii) a ligand, (iii) a fluorescent dye and a
linker, or (iv) a fluorescent dye.
[0072] In a certain embodiment, examples of the conjugate of the present invention include the followings:
(1) a conjugate wherein the anti-human MUC1 antibody Fab fragment is an anti-human
MUC1 antibody Fab fragment comprising a heavy chain fragment comprising a heavy chain
variable region consisting of the amino acid sequence represented by SEQ ID NO: 10 and a light chain comprising a light chain variable region consisting of the amino acid sequence
represented by SEQ ID NO: 12;
(2) the conjugate of (1), wherein the anti-human MUC1 antibody Fab fragment is an anti human MUC1 antibody Fab fragment comprising a heavy chain fragment consisting of the
amino acid sequence represented by SEQ ID NO: 4 and a light chain consisting of the amino
acid sequence represented by SEQ ID NO: 6;
(3) a conjugate wherein the anti-human MUC1 antibody Fab fragment is an anti-human
MUC Iantibody Fab fragment comprising a heavy chain fragment comprising a heavy chain
variable region derived from a heavy chain variable region consisting of the amino acid
sequence represented by SEQ ID NO: 10 by the modification of glutamine at amino acid position 1 of SEQ ID NO: 10 into pyroglutamic acid, and a light chain comprising a light
chain variable region consisting of the amino acid sequence represented by SEQ ID NO: 12;
(4) the conjugate of (2), wherein the anti-human MUC1 antibody Fab fragment is an anti
human MUC1 antibody Fab fragment comprising a heavy chain fragment derived from a
heavy chain fragment consisting of the amino acid sequence represented by SEQ ID NO: 4
by the modification of glutamine at amino acid position 1 of SEQ ID NO: 4 into
pyroglutamic acid, and a light chain consisting of the amino acid sequence represented by
SEQ ID NO: 6;
(5) the conjugate of any of (1) to (4), wherein the labeling moiety is (i) a ligand and a linker, or (ii) a ligand;
(6) the conjugate of any of (1) to (4), wherein the ligand is a group constituted by a chelating agent selected from the group consisting of DFO, DTPA, DTPA-BMA, EOB-DTPA, DO3A,
HP-DO3A and DOTA, and the linker is a linker selected from the group consisting of C(=S)-NH-(1,4-phenylene)-NH-C(=S)-, -CH2 -(1,4-phenylene)-NH-C(=S)- and -C(=O)-(C20
alkylene)-C(=O)-;
(7) the conjugate of (6), wherein the ligand is a group constituted by a chelating agent
selected from the group consisting of DFO, DTPA, and DOTA; (8) the conjugate of (6), wherein the ligand is a group constituted by DFO, and the linker is
C(=S)-NH-(1,4-phenylene)-NH-C(=S)-;
(9) the conjugate according to any of (5) to (8), further comprising a metal; (10) the conjugate of (9), wherein the metal is a metal radioisotope; and
(11) the conjugate of (10), wherein the metal is8 9Zr.
[0073] In a certain embodiment, the conjugate of the present invention is a conjugate wherein the labeling moiety is (i) a ligand and a linker, or (ii) a ligand.
[0074] In a certain embodiment, the conjugate of the present invention is a conjugate
wherein the ligand is a ligand represented by the following formula (A):
[0075] [Chemical Formula 10]
H NH N 0 O O
0 H H3C O (A)
H
wherein the wavy line represents binding to the anti-human MUC1 antibody Fab fragment or the linker.
[0076] In a certain embodiment, the conjugate of the present invention wherein the ligand is a ligand represented by formula (A) is a conjugate wherein the labeling moiety is a ligand
and a linker represented by the following formula (A'):
[0077] [Chemical Formula 11] 0
OH NH N
N-OH (A') 0 NH H3 C O
IH H OH wherein the wavy line represents binding to the anti-human MUC1 antibody Fab fragment,
and the anti-human MUC1 antibody Fab fragment is bound via an amino group thereof to the carbon atom of a labeling moiety terminal C(=S) group.
[0078] In a certain embodiment, the conjugate of the present invention is a conjugate
wherein the labeling moiety is (i) a ligand and a linker, or (ii) a ligand, the conjugate further
comprising a metal. A certain embodiment of the metal is a metal radioisotope. A certain
embodiment of the metal radioisotope is 8 9 Zr
[0079] In an alternative embodiment, the conjugate of the present invention is a conjugate
wherein the labeling moiety is (i) a fluorescent dye and a linker, or (ii) a fluorescent dye.
[0080] In a certain embodiment, the conjugate of the present invention wherein the labeling
moiety comprises a fluorescent dye is a conjugate wherein the fluorescent dye is a fluorescent
dye selected from the group consisting of the following formula (B) and the following
formula (C):
[0081] [Chemical Formula 12] SO 3 Na
NaO3S SO3~
N N+
SO 3 Na
(B)
[0082] [Chemical Formula 13]
SO3 Na
/ \
HN O O N N SO 3 Na /N N-SI--N SO 3Na N N N
c=0 -- 0 si SO 3 Na
(c) wherein the wavy line represents binding to the anti-human MUCl antibody Fab fragment or
the linker.
[0083] In a certain embodiment, the conjugate of the present invention wherein the labeling
moiety is a fluorescent dye represented by formula (B) is a conjugate wherein the wavy line
represents binding to the anti-human MUC Iantibody Fab fragment, and the anti-human
MUC Iantibody Fab fragment is bound via an amino group thereof to the carbon atom of a
labeling moiety terminal C(=O) group.
[0084] In a certain embodiment, the conjugate of the present invention wherein the labeling
moiety is a fluorescent dye represented by formula (C) is a conjugate wherein the wavy line
represents binding to the anti-human MUC1 antibody Fab fragment, and the anti-human
MUC antibody Fab fragment is bound via an amino group thereof to the carbon atom of a
labeling moiety terminal C(=O) group.
[0085] Certain embodiments of the conjugate of the present invention will be further shown
below:
(1) a conjugate wherein the labeling moiety is a ligand and a linker represented by formula
(A'), and the anti-human MUCi antibody Fab fragment is an anti-human MUCi antibody
Fab fragment comprising a heavy chain fragment comprising a heavy chain variable region consisting of the amino acid sequence represented by SEQ ID NO: 10 and a light chain comprising a light chain variable region consisting of the amino acid sequence represented by SEQ ID NO: 12;
(2) the conjugate of (1), wherein the anti-human MUC Iantibody Fab fragment is an anti
human MUC Iantibody Fab fragment comprising a heavy chain fragment consisting of the amino acid sequence represented by SEQ ID NO: 4 and a light chain consisting of the amino
acid sequence represented by SEQ ID NO: 6;
(3) a conjugate wherein the labeling moiety is a ligand and a linker represented by formula
(A'), and the anti-human MUC1 antibody Fab fragment is an anti-human MUC Iantibody Fab fragment comprising a heavy chain fragment comprising a heavy chain variable region
derived from a heavy chain variable region consisting of the amino acid sequence represented
by SEQ ID NO: 10 by the modification of glutamine at amino acid position 1 of SEQ ID NO:
10 into pyroglutamic acid, and a light chain comprising a light chain variable region consisting of the amino acid sequence represented by SEQ ID NO: 12;
(4) the conjugate of (3), wherein the anti-human MUC1 antibody Fab fragment is an anti
human MUC1 antibody Fab fragment comprising a heavy chain fragment derived from a
heavy chain fragment consisting of the amino acid sequence represented by SEQ ID NO: 4
by the modification of glutamine at amino acid position 1 of SEQ ID NO: 4 into
pyroglutamic acid, and a light chain consisting of the amino acid sequence represented by
SEQ ID NO: 6;
(5) the conjugate of (2) or (4) which is the anti-human MUC1 antibody Fab fragment bound
to 1 to 11 labeling moieties;
(6) the conjugate of (2) or (4) which is the anti-human MUCI antibody Fab fragment bound
to 1 to 4 labeling moieties;
(7) the conjugate of any of (1) to (6), further comprising a metal;
(8) the conjugate of (7), wherein the metal is a metal radioisotope;
(9) the conjugate of (8), wherein the metal is 89Zr;
(10) a conjugate wherein the labeling moiety is a fluorescent dye represented by formula (B) or formula (C), and the anti-human MUC Iantibody Fab fragment is an anti-human MUCI antibody Fab fragment comprising a heavy chain fragment comprising a heavy chain variable region consisting of the amino acid sequence represented by SEQ ID NO: 10 and a light chain comprising a light chain variable region consisting of the amino acid sequence represented by SEQ ID NO: 12;
(11) the conjugate of (10), wherein the anti-human MUC1 antibody Fab fragment is an anti
human MUC1 antibody Fab fragment comprising a heavy chain fragment consisting of the
amino acid sequence represented by SEQ ID NO: 4 and a light chain consisting of the amino
acid sequence represented by SEQ ID NO: 6; (12) a conjugate wherein the labeling moiety is a fluorescent dye represented by formula (B)
or formula (C), and the anti-human MUC Iantibody Fab fragment is an anti-human MUCI
antibody Fab fragment comprising a heavy chain fragment comprising a heavy chain variable
region derived from a heavy chain variable region consisting of the amino acid sequence represented by SEQ ID NO: 10 by the modification of glutamine at amino acid position 1 of
SEQ ID NO: 10 into pyroglutamic acid, and a light chain comprising a light chain variable
region consisting of the amino acid sequence represented by SEQ ID NO: 12;
(13) the conjugate of (12), wherein the anti-human MUC1 antibody Fab fragment is an anti
human MUC1 antibody Fab fragment comprising a heavy chain fragment derived from a
heavy chain fragment consisting of the amino acid sequence represented by SEQ ID NO: 4
by the modification of glutamine at amino acid position 1 of SEQ ID NO: 4 into
pyroglutamic acid, and a light chain consisting of the amino acid sequence represented by
SEQ ID NO: 6;
(14) the conjugate of any of (10) to (13), wherein the labeling moiety is a fluorescent dye
represented by formula (C);
(15) the conjugate of (14) which is the anti-human MUC Iantibody Fab fragment bound to 1
to 11 labeling moieties;
(16) the conjugate of (15) which is the anti-human MUC1 antibody Fab fragment bound to 1
to 5 labeling moieties;
(17) the conjugate of any of (10) to (13), wherein the labeling moiety is a fluorescent dye
represented by formula (B); (18) the conjugate of (17) which is the anti-human MUC1 antibody Fab fragment bound to 1
to 11 labeling moieties; and
(19) the conjugate of (18) which is the anti-human MUC Iantibody Fab fragment bound to 1 to 5 labeling moieties.
[0086] In an alternative embodiment, the conjugate of the present invention is a conjugate
represented by the following formula (I):
[0087] [Chemical Formula 14]
(L-X)p-Ab(I wherein Ab represents the anti-human MUC1 antibody Fab fragment, L represents (i) a ligand or (ii) a fluorescent dye,
X represents a linker or a bond, and
p is a natural number of 1 to 27. A certain embodiment of p is a natural number of I to 23. A certain embodiment is a natural number of 1 to 15. A certain embodiment is a natural number of 1 to 11. A certain embodiment is a natural number of 1 to 9. A certain
embodiment is a natural number of 1 to 7. A certain embodiment is a natural number of 1 to 5. A certain embodiment is a natural number of 1 to 4.
[0088] In a certain embodiment, the conjugate of the present invention is a conjugate of
formula (I), the conjugate further comprising a metal. A certain embodiment of the metal is a metal radioisotope. A certain embodiment of the metal radioisotope is 89Zr.
[0089] In a certain embodiment, the conjugate of formula (I) is the conjugate of the present
invention wherein the labeling moiety is a ligand and a linker represented by formula (A').
In a certain embodiment, this conjugate is a conjugate represented by the following formula
(II):
[0090] [Chemical Formula 15]
H NH N
0 1 H
0 NH H 3 CIO0 M ,Ab (I
0~~ H H H
wherein Ab represents the anti-human MUC1 antibody Fab fragment, and
p is a natural number of 1 to 27. A certain embodiment of p is a natural number of 1 to 23.
A certain embodiment is a natural number of 1 to 15. A certain embodiment is a natural number of 1 to 11. A certain embodiment is a natural number of 1 to 9. A certain
embodiment is a natural number of 1 to 7. A certain embodiment is a natural number of 1 to 5. A certain embodiment is a natural number of 1 to 4. Ab is bound via an amino group thereof to the carbon atom of a labeling moiety terminal
C(=S) group.
[0091] Ina certain embodiment, the conjugate of the present invention is a conjugate of
formula (II), the conjugate further comprising a metal. A certain embodiment of the metal
is a metal radioisotope. A certain embodiment of the metal radioisotope is 89Zr.
[0092] In a certain embodiment, the conjugate of formula (I) is the conjugate of the present invention wherein the labeling moiety is a fluorescent dye represented by formula (B). In a
certain embodiment, the conjugate is a conjugate represented by the following formula (III):
[0093] [Chemical Formula 16]
SO 3 Na
Na3S S03~
/ O+
SO 3 Na o=-c aAb
wherein Ab represents the anti-human MUC1 antibody Fab fragment, and
p is a natural number of 1 to 27. A certain embodiment of p is a natural number of 1 to 23.
A certain embodiment is a natural number of I to 15. A certain embodiment is a natural
number of 1 to 11. A certain embodiment is a natural number of 1 to 9. A certain
embodiment is a natural number of 1 to 7. A certain embodiment is a natural number of 1 to
5. A certain embodiment is a natural number of 1 to 4.
Ab is bound via an amino group thereof to the carbon atom of a labeling moiety terminal
C(=O) group.
[0094] In a certain embodiment, the conjugate of formula (I) is the conjugate of the present
invention wherein the labeling moiety is a fluorescent dye represented by formula (C). In a
certain embodiment, this conjugate is a conjugate represented by the following formula (IV):
[0095] [Chemical Formula 17]
SO 3Na
HN/O O N / \ON N SO 3Na /N
/N Na _SO 3Na NN
Ab -- -C=0 SosNa p
(IV) wherein Ab represents the anti-human MUC1 antibody Fab fragment, and
p is a natural number of 1 to 27. A certain embodiment of p is a natural number of 1 to 23.
A certain embodiment is a natural number of 1 to 15. A certain embodiment is a natural
number of 1 to 11. A certain embodiment is a natural number of 1 to 9. A certain
embodiment is a natural number of 1 to 7. A certain embodiment is a natural number of 1 to
5. A certain embodiment is a natural number of 1 to 4.
Ab is bound via an amino group thereof to the carbon atom of a labeling moiety terminal
C(=O) group.
[0096] In a certain embodiment, the conjugate of the present invention is the anti-human
MUC1 antibody Fab fragment of the present invention labeled with a detectable molecule.
The anti-human MUC1 antibody Fab fragment of the present invention labeled with a
detectable molecule is the anti-human MUC antibody Fab fragment of the present invention
and the detectable molecule linked through a covalent bond directly or via an appropriate
linker. In the present specification, the detectable molecule means every moiety detectable
in an imaging diagnosis technique known in the art. When the imaging diagnosis technique
is, for example, fluorescence imaging, the detectable molecule is a fluorescent dye. When
the imaging diagnosis technique is PET, the detectable molecule is a compound imageable by
PET. A certain embodiment is a compound comprising a ligand labeled with a
radionuclide, or a sugar residue labeled with a nonmetal radionuclide. A certain
embodiment of the compound comprising a ligand labeled with a radionuclide is a ligand that
has formed a chelate complex with a metal radioisotope. When the imaging diagnosis
technique is MRI, the detectable molecule is a compound detectable by the MRI technique.
A certain embodiment is a compound comprising a labeled ligand having a paramagnetic
metal ion. A certain embodiment of the compound comprising a labeled ligand having a paramagnetic metal ion is a ligand that has formed a chelate complex with a paramagnetic
metal ion.
[0097] When the anti-human MUC1 antibody Fab fragment of the present invention labeled
with a detectable molecule is used in the context of a detectable molecule, the compound imageable by PET is referred to as a PET tracer, and the compound detectable by the MRI
technique is referred to as a MRI contrast medium.
[0098] Examples of certain embodiments of the anti-human MUC1 antibody Fab fragment
of the present invention labeled with a detectable molecule include the followings: (1) an anti-human MUC1 antibody Fab fragment wherein the detectable molecule is a
fluorescent dye, a PET tracer, or a MRI contrast medium; (2) the anti-human MUC1 antibody Fab fragment of (1), wherein the detectable molecule is a fluorescent dye;
(3) the anti-human MUC1 antibody Fab fragment of (2), wherein the detectable molecule is a
fluorescent dye represented by formula (B); (4) the anti-human MUC1 antibody Fab fragment of (2), wherein the detectable molecule is a
fluorescent dye represented by formula (C);
(5) the anti-human MUC1 antibody Fab fragment of (1), wherein the detectable molecule is a
PET tracer or a MRI contrast medium;
(6) an anti-human MUC1 antibody Fab fragment wherein the detectable molecule is a MRI
contrast medium comprising a ligand represented by formula (A) and a paramagnetic metal
ion, or a PET tracer comprising the ligand and a metal radioisotope; and
(7) the anti-human MUC1 antibody Fab fragment of (6), wherein the detectable molecule and
the linker are a MRI contrast medium comprising a ligand and a linker represented by
formula (A') and a paramagnetic metal ion, or a PET tracer comprising the ligand and the
linker and a metal radioisotope.
[0099] The method mentioned above can be employed for the linking of the anti-human
MUCl antibody Fab fragment of the present invention to the detectable molecule.
[0100] The conjugate of the present invention also includes a conjugate which is a mixture of a plurality of conjugates of the present invention. For example, a conjugate which is
mixture of a conjugate comprising a labeling moiety and a non-posttranslationally-modified anti-human MUCl antibody Fab fragment of the present invention, and a conjugate
comprising a labeling moiety and the anti-human MUC1 antibody Fab fragment of the present invention resulting from the posttranslational modification of the anti-human MUC1
antibody Fab fragment is also included in the conjugate of the present invention.
[0101] Certain embodiments of the conjugate of the present invention which is a mixture of
a plurality of conjugates of the present invention will be shown below: (1) a conjugate which is a mixture of a conjugate wherein the labeling moiety is a ligand and
a linker represented by formula (A'), and the anti-human MUC1 antibody Fab fragment is an
anti-human MUC Iantibody Fab fragment comprising a heavy chain fragment consisting of the amino acid sequence represented by SEQ ID NO: 4 and a light chain consisting of the
amino acid sequence represented by SEQ ID NO: 6, and a conjugate wherein the labeling
moiety is a ligand and a linker represented by formula (A'), and the anti-human MUC1 antibody Fab fragment is an anti-human MUC Iantibody Fab fragment comprising a heavy
chain fragment derived from a heavy chain fragment consisting of the amino acid sequence
represented by SEQ ID NO: 4 by the modification of glutamine at amino acid position 1 of
SEQ ID NO: 4 into pyroglutamic acid, and a light chain consisting of the amino acid
sequence represented by SEQ ID NO: 6;
(2) the conjugate of (1), further comprising a metal;
(3) the conjugate of (2), wherein the metal is a metal radioisotope;
(4) the conjugate of (3), wherein the metal is 89Zr;
(5) a conjugate which is a mixture of a conjugate wherein the labeling moiety is a fluorescent
dye represented by formula (B), and the anti-human MUCl antibody Fab fragment is an anti
human MUC I antibody Fab fragment comprising a heavy chain fragment consisting of the
amino acid sequence represented by SEQ ID NO: 4 and a light chain consisting of the amino
acid sequence represented by SEQ ID NO: 6, and a conjugate wherein the labeling moiety is
a fluorescent dye represented by formula (B), and the anti-human MUC Iantibody Fab
fragment is an anti-human MUC1 antibody Fab fragment comprising a heavy chain fragment
derived from a heavy chain fragment consisting of the amino acid sequence represented by
SEQ ID NO: 4 by the modification of glutamine at amino acid position 1 of SEQ ID NO: 4
into pyroglutamic acid, and a light chain consisting of the amino acid sequence represented
by SEQ ID NO: 6; and
(6) a conjugate which is a mixture of a conjugate wherein the labeling moiety is a fluorescent
dye represented by formula (C), and the anti-human MUC Iantibody Fab fragment is an anti
human MUC1 antibody Fab fragment comprising a heavy chain fragment consisting of the
amino acid sequence represented by SEQ ID NO: 4 and a light chain consisting of the amino
acid sequence represented by SEQ ID NO: 6, and a conjugate wherein the labeling moiety is
a fluorescent dye represented by formula (C), and the anti-human MUC1 antibody Fab
fragment is an anti-human MUC antibody Fab fragment comprising a heavy chain fragment
derived from a heavy chain fragment consisting of the amino acid sequence represented by
SEQ ID NO: 4 by the modification of glutamine at amino acid position 1 of SEQ ID NO: 4
into pyroglutamic acid, and a light chain consisting of the amino acid sequence represented
by SEQ ID NO: 6.
[0102] <Polynucleotide of present invention>
The polynucleotide of the present invention includes a polynucleotide comprising a
nucleotide sequence encoding the heavy chain fragment of the anti-human MUC1 antibody
Fab fragment of the present invention, and a polynucleotide comprising a nucleotide
sequence encoding the light chain of the anti-human MUCi antibody Fab fragment of the present invention.
[0103] In one embodiment, the polynucleotide of the present invention is apolynucleotide
comprising a nucleotide sequence encoding a heavy chain fragment comprising a heavy chain
variable region consisting of the amino acid sequence represented by SEQ ID NO: 8, or a
polynucleotide comprising a nucleotide sequence encoding a heavy chain fragment
comprising a heavy chain variable region consisting of the amino acid sequence represented
by SEQ ID NO: 10.
[0104] Examples of the polynucleotide comprising a nucleotide sequence encoding a heavy chain fragment comprising a heavy chain variable region consisting of the amino acid
sequence represented by SEQ ID NO: 8 include a polynucleotide comprising the nucleotide
sequence represented by SEQ ID NO: 7. Examples of the polynucleotide comprising a
nucleotide sequence encoding a heavy chain fragment comprising a heavy chain variable region consisting of the amino acid sequence represented by SEQ ID NO: 10 include a
polynucleotide comprising the nucleotide sequence represented by SEQ ID NO: 9.
[0105] In one embodiment, the polynucleotide of the present invention is apolynucleotide comprising a nucleotide sequence encoding a heavy chain fragment consisting of the amino
acid sequence represented by SEQ ID NO: 2 or a polynucleotide comprising a nucleotide
sequence encoding a heavy chain fragment consisting of the amino acid sequence represented
by SEQ ID NO: 4.
[0106] Examples of the polynucleotide comprising a nucleotide sequence encoding a heavy
chain fragment consisting of the amino acid sequence represented by SEQ ID NO: 2 include
a polynucleotide comprising the nucleotide sequence represented by SEQ ID NO: 1.
Examples of the polynucleotide comprising a nucleotide sequence encoding a heavy chain
fragment consisting of the amino acid sequence represented by SEQ ID NO: 4 include a
polynucleotide comprising the nucleotide sequence represented by SEQ ID NO: 3.
[0107] In one embodiment, the polynucleotide of the present invention is apolynucleotide comprising a nucleotide sequence encoding a light chain comprising a light chain variable
region consisting of the amino acid sequence represented by SEQ ID NO: 12.
[0108] Examples of the polynucleotide comprising a nucleotide sequence encoding alight chain comprising a light chain variable region consisting of the amino acid sequence
represented by SEQ ID NO: 12 include a polynucleotide comprising the nucleotide sequence
represented by SEQ ID NO: 11.
[0109] In one embodiment, the polynucleotide of the present invention is apolynucleotide
comprising a nucleotide sequence encoding a light chain consisting of the amino acid
sequence represented by SEQ ID NO: 6.
[0110] Examples of the polynucleotide comprising a nucleotide sequence encoding alight
chain consisting of the amino acid sequence represented by SEQ ID NO: 6 include a
polynucleotide comprising the nucleotide sequence represented by SEQ ID NO: 5.
[0111] The polynucleotide of the present invention is synthesizable through the use of a
gene synthesis method known in the art on the basis of nucleotide sequences designed from
the amino acid sequences of the heavy chain fragment and the light chain of the anti-human
MUC1 antibody Fab fragment of the present invention. Various methods known to those
skilled in the art, such as methods for synthesizing an antibody gene described in
International Publication No. WO 90/07861 can be used as such gene synthesis methods.
[0112] <Expression vector of present invention>
The expression vector of the present invention includes an expression vector
comprising a polynucleotide comprising a nucleotide sequence encoding the heavy chain
fragment of the anti-human MUC1 antibody Fab fragment of the present invention, an
expression vector comprising a polynucleotide comprising a nucleotide sequence encoding
the light chain of the anti-human MUC1 antibody Fab fragment of the present invention, and
an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding
the heavy chain fragment of the anti-human MUCi antibody Fab fragment of the present
invention and a polynucleotide comprising a nucleotide sequence encoding the light chain of
the anti-human MUC1 antibody Fab fragment of the present invention.
[0113] The expression vector of the present invention preferably includes an expression
vector comprising a polynucleotide comprising a nucleotide sequence encoding a heavy chain fragment consisting of the amino acid sequence represented by SEQ ID NO: 4, an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding a light chain consisting of the amino acid sequence represented by SEQ ID NO: 6, and an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding a heavy chain fragment consisting of the amino acid sequence represented by SEQ ID NO: 4 and a polynucleotide comprising a nucleotide sequence encoding a light chain consisting of the amino acid sequence represented by SEQ ID NO: 6.
[0114] The expression vector of the present invention is not particularly limited as long as a polypeptide encoded by the polynucleotide of the present invention can be produced in
various host cells of prokaryotic cells and/or eukaryotic cells. Examples of such an expression vector include plasmid vectors and virus vectors (e.g., adenovirus and retrovirus).
Preferably, pEE6.4 or pEE12.4 (Lonza Ltd.) can be used.
[0115] The expression vector of the present invention can comprise a promoter operably
linked to a gene encoding the heavy chain fragment and/or the light chain in the
polynucleotide of the present invention. Examples of the promoter for expressing the Fab
fragment of the present invention in a host cell include Trp promoter, lac promoter, recA
promoter, XPL promoter, lpp promoter, and tac promoter when the host cell is a bacterium of the genus Escherichia. Examples of the promoter for expression in yeasts include PH05
promoter, PGK promoter, GAP promoter, and ADH promoter. Examples of the promoter
for expression in bacteria of the genus Bacillus include SLO1 promoter, SP02 promoter, and penP promoter. Examples thereof include promoters derived from viruses such as CMV, RSV, and SV40, retrovirus promoter, actin promoter, EF (elongation factor)1 Upromoter,
and heat shock promoter when the host is a eukaryotic cell such as a mammalian cell.
[0116] In the case of using a bacterium, particularly, E. coli, as a host cell, the expression
vector of the present invention can further comprise a start codon, a stop codon, a terminator
region and a replicable unit. On the other hand, in the case of using a yeast, an animal cell or an insect cell as a host, the expression vector of the present invention can comprise a start
codon and a stop codon. In this case, an enhancer sequence, 5' and 3'untranslated regions of a gene encoding the heavy chain fragment and/or the light chain of the present invention, a secretion signal sequence, a splicing junction, a polyadenylation site, or a replicable unit, etc.
maybe contained therein. Also, a selective marker usually used (e.g., tetracycline
resistance gene, ampicillin resistance gene, kanamycin resistance gene, neomycin resistance
gene, dihydrofolate reductase gene) may be contained therein according to a purpose.
[0117] <Transformed host cell of present invention>
The transformed host cell of the present invention includes a host cell transformed
with the expression vector of the present invention, selected from the group consisting of the
following (a) to (d):
(a) a host cell transformed with an expression vector comprising a polynucleotide comprising
a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC1 antibody
Fab fragment of the present invention;
(b) a host cell transformed with an expression vector comprising a polynucleotide comprising
a nucleotide sequence encoding the light chain of the anti-human MUC1 antibody Fab
fragment of the present invention;
(c) a host cell transformed with an expression vector comprising a polynucleotide comprising
a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC1 antibody
Fab fragment of the present invention and a polynucleotide comprising a nucleotide sequence
encoding the light chain of the anti-human MUC Iantibody Fab fragment of the present
invention; and
(d) a host cell transformed with an expression vector comprising a polynucleotide comprising
a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC1 antibody
Fab fragment of the present invention and an expression vector comprising a polynucleotide
comprising a nucleotide sequence encoding the light chain of the anti-human MUC1 antibody
Fab fragment of the present invention.
[0118] In one embodiment, the transformed host cell of the present invention is a host cell
transformed with the expression vector of the present invention, selected from the group
consisting of the following (a) to (d):
(a) a host cell transformed with an expression vector comprising a polynucleotide comprising
a nucleotide sequence encoding a heavy chain fragment consisting of the amino acid
sequence represented by SEQ ID NO: 4;
(b) a host cell transformed with an expression vector comprising a polynucleotide comprising
a nucleotide sequence encoding a light chain consisting of the amino acid sequence
represented by SEQ ID NO: 6;
(c) a host cell transformed with an expression vector comprising a polynucleotide comprising
a nucleotide sequence encoding a heavy chain fragment consisting of the amino acid sequence represented by SEQ ID NO: 4 and a polynucleotide comprising a nucleotide
sequence encoding a light chain consisting of the amino acid sequence represented by SEQ
ID NO: 6; and
(d) a host cell transformed with an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding a heavy chain fragment consisting of the amino acid
sequence represented by SEQ ID NO: 4 and an expression vector comprising a
polynucleotide comprising a nucleotide sequence encoding a light chain consisting of the
amino acid sequence represented by SEQ ID NO: 6.
[0119] The host cell to be transformed is not particularly limited as long as it is compatible with the expression vector used and can be transformed with the expression vector to express
the Fab fragment. Examples thereof include various cells such as natural cells and
artificially established cells usually used in the technical field of the present invention (e.g.,
bacteria (bacteria of the genus Escherichiaand bacteria of the genus Bacillus), yeasts (the
genus Saccharomyces, the genus Pichia, etc.), animal cells and insect cells (e.g., Sf9)), and
mammalian cell lines (e.g., cultured cells such as CHO-KlSV cells, CHO-DG44 cells, and
293 cells). The transformation itself can be performed by a known method, for example, a
calcium phosphate method or an electroporation method.
[0120] <Method for producing anti-human MUC1 antibody Fab fragment according to
present invention>
The method for producing an anti-human MUC Iantibody Fab fragment according to the present invention comprises the step of culturing the transformed host cell of the present invention to express the anti-human MUC1 antibody Fab fragment.
[0121] In one embodiment, the transformed host cell of the present invention to be cultured
in the method for producing an anti-human MUC Iantibody Fab fragment according to the
present invention is selected from the group consisting of the following (a) to (c):
(a) a host cell transformed with an expression vector comprising a polynucleotide comprising
a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC1 antibody
Fab fragment of the present invention and a polynucleotide comprising a nucleotide sequence encoding the light chain of the anti-human MUC Iantibody Fab fragment of the present invention;
(b) a host cell transformed with an expression vector comprising a polynucleotide comprising
a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC Iantibody Fab fragment of the present invention and an expression vector comprising a polynucleotide
comprising a nucleotide sequence encoding the light chain of the anti-human MUC1 antibody
Fab fragment of the present invention; and
(c) a host cell transformed with an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC Iantibody
Fab fragment of the present invention, and a host cell transformed with an expression vector
comprising a polynucleotide comprising a nucleotide sequence encoding the light chain of
the anti-human MUC Iantibody Fab fragment of the present invention.
[0122] A certain form of the transformed host cell of the present invention to be cultured in
the method for producing an anti-human MUC Iantibody Fab fragment according to the
present invention is selected from the group consisting of the following (a) to (c):
(a) a host cell transformed with an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding a heavy chain fragment consisting of the amino acid
sequence represented by SEQ ID NO: 4 and a polynucleotide comprising a nucleotide
sequence encoding a light chain consisting of the amino acid sequence represented by SEQ
ID NO: 6;
(b) a host cell transformed with an expression vector comprising a polynucleotide comprising
a nucleotide sequence encoding a heavy chain fragment consisting of the amino acid
sequence represented by SEQ ID NO: 4 and an expression vector comprising a
polynucleotide comprising a nucleotide sequence encoding a light chain consisting of the
amino acid sequence represented by SEQ ID NO: 6; and
(c) a host cell transformed with an expression vector comprising a polynucleotide comprising
a nucleotide sequence encoding a heavy chain fragment consisting of the amino acid
sequence represented by SEQ ID NO: 4, and a host cell transformed with an expression
vector comprising a polynucleotide comprising a nucleotide sequence encoding a light chain
consisting of the amino acid sequence represented by SEQ ID NO: 6.
[0123] Preferably, the transformed host cell of the present invention used is a host cell
transformed with an expression vector comprising a polynucleotide comprising a nucleotide
sequence encoding the heavy chain fragment of the anti-human MUC1 antibody Fab
fragment of the present invention and a polynucleotide comprising a nucleotide sequence
encoding the light chain of the anti-human MUC1 antibody Fab fragment of the present
invention, or a host cell transformed with an expression vector comprising a polynucleotide
comprising a nucleotide sequence encoding the heavy chain fragment of the anti-human
MUC1 antibody Fab fragment of the present invention and an expression vector comprising a
polynucleotide comprising a nucleotide sequence encoding the light chain of the anti-human
MUC1 antibody Fab fragment of the present invention.
[0124] In the method for producing an anti-human MUCi antibody Fab fragment according
to the present invention, the transformed host cell can be cultured in a nutrient medium.
The nutrient medium preferably contains a carbon source, an inorganic nitrogen source or an
organic nitrogen source necessary for the growth of the transformed host cell. Examples of
the carbon source include glucose, dextran, soluble starch, and sucrose. Examples of the
inorganic nitrogen source or the organic nitrogen source include ammonium salts, nitrates,
amino acids, corn steep liquor, peptone, casein, meat extracts, soymeal, and potato extracts.
Also, other nutrients (e.g., inorganic salts (e.g., calcium chloride, sodium dihydrogen phosphate, and magnesium chloride), vitamins, and antibiotics (e.g., tetracycline, neomycin, ampicillin, and kanamycin)) may be contained therein, if desired.
[0125] The culture itself of the transformed host cell is performed by a known method.
Culture conditions, for example, temperature, medium pH and culture time, are appropriately
selected. When the host is, for example, an animal cell, MEM medium (Science; 1952; 122:
501), DMEM medium (Virology; 1959; 8: 396-97), RPMIl640 medium (J. Am. Med.
Assoc.; 1967; 199: 519-24), 199 medium (Proc. Soc. Exp. Biol. Med.; 1950; 73:1-8), or the like containing approximately 5 to 20% of fetal bovine serum can be used as a medium.
The medium pH is preferably approximately 6 to 8. The culture is usually performed at approximately 30 to 40°C for approximately 15 to 336 hours, and aeration or stirring can also
be performed, if necessary. When the host is an insect cell, examples thereof include Grace's medium (PNAS; 1985; 82: 8404-8) containing fetal bovine serum. Its pH is
preferably approximately 5 to 8. The culture is usually performed at approximately 20 to 40°C for 15 to 100 hours, and aeration or stirring can also be performed, if necessary.
When the host is a bacterium, an actinomycete, a yeast, or a filamentous fungus, for example, a liquid medium containing the nutrient source described above is appropriate. A medium
of pH 5 to 8 is preferred. When the host is E. coli, preferred examples of the medium
include LB medium and M9 medium (Miller et al., Exp. Mol. Genet, Cold Spring Harbor Laboratory; 1972: 431). In such a case, the culture can usually be performed at 14 to 43°C
for approximately 3 to 24 hours with aeration or stirring, if necessary. When the host is a
bacterium of the genus Bacillus, it can usually be performed at 30 to 40°C for approximately
16 to 96 hours with aeration or stirring, if necessary. When the host is a yeast, examples of
the medium include Burkholder minimum medium (PNAS; 1980; 77: 4505-8). Its pH is desirably 5 to 8. The culture is usually performed at approximately 20 to 35°C for
approximately 14 to 144 hours, and aeration or stirring can also be performed, if necessary.
[0126] The method for producing an anti-human MUCI antibody Fab fragment according
to the present invention can comprise the step of recovering, preferably isolating or purifying,
the expressed anti-human MUC1 antibody Fab fragment, in addition to the step of culturing the transformed host cell of the present invention to express the anti-human MUCantibody
Fab fragment. Examples of the isolation or purification method include: methods exploiting
solubility, such as salting out and a solvent precipitation method; methods exploiting
difference in molecular weight, such as dialysis, ultrafiltration, gel filtration, and sodium
dodecyl sulfate-polyacrylamide gel electrophoresis; methods exploiting charge, such as ion
exchange chromatography and hydroxylapatite chromatography; methods exploiting specific
affinity, such as affinity chromatography; methods exploiting difference in hydrophobicity,
such as reverse-phase high-performance liquid chromatography; and methods exploiting
difference in isoelectric point, such as isoelectric focusing.
[0127] <Method for producing conjugate according to present invention>
The method for producing a conjugate according to the present invention comprises
the step of covalently binding the anti-human MUC Iantibody Fab fragment of the present
invention to a labeling moiety. The method for producing a conjugate according to the
present invention may also comprise the steps of: culturing the transformed host cell of the
present invention to express the anti-human MUC1 antibody Fab fragment; and covalently
binding the Fab fragment to a labeling moiety. The method for producing a conjugate
according to the present invention may also comprise the steps of: culturing the transformed
host cell of the present invention to express the anti-human MUC1 antibody Fab fragment;
recovering the expressed Fab fragment; and covalently binding the Fab fragment to a labeling
moiety. The method for producing a conjugate according to the present invention may
further comprise the step of adding a metal. The linker, chelating agent, metal, or
fluorescent dye, etc., and linking method used can employ those described in <Conjugate of
present invention>.
[0128] In one embodiment, the method for producing a conjugate according to the present
invention is a method comprising the steps of: culturing the transformed host cell of the
present invention to express the anti-human MUC1 antibody Fab fragment; and covalently
binding the Fab fragment to a labeling moiety. A certain embodiment of the method for
producing a conjugate according to the present invention is a method comprising the steps of: culturing the transformed host cell of the present invention to express the anti-human MUC1 antibody Fab fragment; recovering the expressed Fab fragment; and covalently binding the
Fab fragment to a labeling moiety.
[0129] A certain embodiment of the method for producing a conjugate according to the
present invention is a method comprising the steps of: culturing the transformed host cell of
the present invention to express the anti-human MUC1 antibody Fab fragment; and i) binding
the Fab fragment via a linker to a ligand or ii) covalently binding the Fab fragment directly to
a ligand. A certain embodiment of the method for producing a conjugate according to the
present invention is a method comprising the steps of: culturing the transformed host cell of
the present invention to express the anti-human MUC1 antibody Fab fragment; recovering
the expressed Fab fragment; and i) binding the Fab fragment via a linker to a ligand or ii)
covalently binding the Fab fragment directly to a ligand.
[0130] A certain embodiment of the method for producing a conjugate according to the
present invention is a method comprising the steps of: culturing the transformed host cell of
the present invention to express the anti-human MUC1 antibody Fab fragment; i) binding the
Fab fragment via a linker to a ligand or ii) covalently binding the Fab fragment directly to a
ligand; and labeling the ligand of the conjugate with a metal (i.e., forming a chelate
complex). A certain embodiment of the method for producing a conjugate according to the
present invention is a method comprising the steps of: culturing the transformed host cell of
the present invention to express the anti-human MUC1 antibody Fab fragment; recovering
the expressed Fab fragment; i) binding the Fab fragment via a linker to a ligand or ii)
covalently binding the Fab fragment directly to a ligand; and labeling the ligand of the
conjugate with a metal.
[0131] A certain embodiment of the method for producing a conjugate according to the
present invention is a method comprising the steps of: culturing the transformed host cell of
the present invention to express the anti-human MUC Iantibody Fab fragment; i) binding the
Fab fragment via a linker to a ligand or ii) covalently binding the Fab fragment directly to a
ligand; and labeling the ligand of the conjugate with a metal radioisotope (i.e., forming a chelate complex). A certain embodiment of the method for producing a conjugate according to the present invention is a method comprising the steps of: culturing the transformed host cell of the present invention to express the anti-human MUCl antibody Fab fragment; recovering the expressed Fab fragment; i) binding the Fab fragment via a linker to a ligand or ii) covalently binding the Fab fragment directly to a ligand; and labeling the ligand of the conjugate with a metal radioisotope.
[0132] A certain embodiment of the method for producing a conjugate according to the
present invention is a method comprising the steps of: culturing the transformed host cell of
the present invention to express the anti-human MUC antibody Fab fragment; and i) binding
the Fab fragment via a linker to a fluorescent dye or ii) covalently binding the Fab fragment
directly to a fluorescent dye. A certain embodiment of the method for producing a
conjugate according to the present invention is a method comprising the steps of: culturing
the transformed host cell of the present invention to express the anti-human MUC Iantibody
Fab fragment; recovering the expressed Fab fragment; and i) binding the Fab fragment via a
linker to a fluorescent dye or ii) covalently binding the Fab fragment directly to a fluorescent
dye.
[0133] A certain embodiment of the method for producing a conjugate according to the
present invention is a method comprising the steps of: culturing the transformed host cell of
the present invention to express the anti-human MUC1 antibody Fab fragment; and labeling
the Fab fragment with a detectable molecule. A certain embodiment of the method for
producing a conjugate according to the present invention is a method comprising the steps of:
culturing the transformed host cell of the present invention to express the anti-human MUC1
antibody Fab fragment; recovering the expressed Fab fragment; and labeling the Fab
fragment with a detectable molecule.
[0134] The method for producing a conjugate according to the present invention maybe
carried out as a method comprising two or more of the steps defined above as a series of steps
or may be carried out as a method comprising at least one of the steps defined above. For
example, a method comprising the step of binding the anti-human MUC Iantibody Fab fragment of the present invention to a labeling moiety, and a method comprising the step of labeling the anti-human MUC Iantibody Fab fragment of the present invention bound to the labeling moiety with a metal are also included in the method for producing a conjugate according to the present invention. Also, the method for producing a conjugate according to the present invention includes a method having a different order of steps. For example, a method comprising labeling a chelating agent with a metal, and then covalently binding the chelating agent to the anti-human MUCl antibody Fab fragment of the present invention is also included in the method for producing a conjugate according to the present invention.
[0135] <Composition for diagnosis and diagnosis method>
The present invention relates to a composition for diagnosis comprising the
conjugate of the present invention comprising a metal or a fluorescent dye (hereinafter,
referred to as the detectable conjugate of the present invention). The composition for
diagnosis of the present invention may comprise one or more conjugate of the present
invention. Specifically, the composition for diagnosis of the present invention may
comprise one conjugate of the present invention, or may comprise two or more conjugates of
the present invention in combination. The detectable conjugate of the present invention can
be formulated according to a routine method and utilized as an early diagnostic drug, a
staging drug or a intraoperative diagnostic drug (particularly, a cancer diagnostic drug).
The intraoperative diagnostic drug means a diagnostic drug capable of identifying a lesion
site during operation such as surgery or endoscopic operation and examining its nature. In
the case of using the composition for diagnosis of the present invention as an intraoperative
diagnostic drug, the composition for diagnosis is administered to a patient, for example, 2 to
32 hours, 6 to 24 hours in a certain embodiment, or 2 hours in another embodiment, before
operation.
[0136] The early diagnostic drug means a diagnostic drug aimed atperforming diagnosis
when no condition is observed or at an early stage. For example, for cancers, it means a
diagnostic drug that is used when no condition is observed or at stage 0 or stage 1.
[0137] The staging drug means a diagnostic drug capable of examining the degree of progression of a condition. For example, for cancers, it means a diagnostic drug capable of examining the stage thereof.
[0138] The cancer expected to be able to be diagnosed by the composition for diagnosis of the present invention is a cancer expressing human MUC1. Examples of a certain
embodiment include breast cancer, lung cancer, colorectal cancer, bladder cancer, skin
cancer, thyroid gland cancer, stomach cancer, pancreatic cancer, kidney cancer, ovary cancer
and uterine cervical cancer. Preferably, the cancer is breast cancer or bladder cancer.
[0139] The amount of the conjugate of the present invention added for the formulation of the composition for diagnosis of the present invention differs depending on the degree of
symptoms or age of a patient, the dosage form of a preparation used, or the binding titer of
the Fab fragment, etc. For example, approximately 0.001 mg/kg to 100 mg/kg based on the
mass of the Fab fragment can be used per unit body weight of a patient.
[0140] Examples of the dosage form of the composition for diagnosis of the present
invention can include parenteral agents such as injections and agents for drip infusion. Administration can be performed by intravenous injection, local intramuscular injection to a
target tissue, subcutaneous injection, intravesical administration, or the like. For the
formulation, a carrier or an additive suitable for these dosage forms can be used in a pharmaceutically acceptable range. The type of the pharmaceutically acceptable carrier or
additive is not particularly limited, and a carrier or an additive well known to those skilled in
the art can be used.
[0141] The present invention also relates to use of the detectable conjugate of the present
invention for the production of a composition for the early diagnosis, a composition for the
staging or a composition for the intraoperative diagnosis of a cancer. The present invention
also relates to the detectable conjugate of the present invention for use in the early diagnosis,
staging or intraoperative diagnosis of a cancer.
[0142] Further, the present invention also relates to a method for diagnosing a cancer, comprising preoperatively or intraoperatively administering the detectable conjugate of the
present invention to a subject. In this context, the "subject" is a human or any of other mammals in need of receiving the diagnosis. A certain embodiment is a human in need of receiving the diagnosis. The effective amount of the detectable conjugate of the present invention in the diagnosis method of the present invention may be the same amount as the effective amount of the conjugate of the present invention for the formulation described above. In the diagnosis method of the present invention, the detectable conjugate of the present invention is preferably administered by local intramuscular injection to a target tissue, subcutaneous injection, or the like. In the diagnosis method of the present invention, in the case of preoperatively administering the conjugate of the present invention, the conjugate is administered to a patient, for example, 2 to 48 hours, 6 to 24 hours in a certain embodiment, and 2 hours in another embodiment before operation.
[0143] In an alternative embodiment, the present invention also relates to use of the anti
human MUC1 antibody Fab fragment of the present invention for the production of the
conjugate of the present invention. In a certain embodiment, the present invention also
relates to use of the anti-human MUC1 antibody Fab fragment of the present invention for
the production of a composition for diagnosis comprising the conjugate of the present
invention.
[0144] As for a embodiment in which the composition for diagnosis of the present
invention comprising a metal radioisotope is provided, it may be labeled with the metal
radioisotope immediately before use or may be provided as a composition for diagnosis
comprising the metal radioisotope.
[0145] <Composition for treatment and treatment method>
The present invention includes a pharmaceutical composition comprising one or
more conjugate of the present invention and a pharmaceutically acceptable excipient.
Specifically, the composition for treatment of the present invention may comprise one
conjugate of the present invention, or may comprise two or more conjugates of the present
invention in combination. The conjugate of the present invention can be used in the
preparation of a pharmaceutical composition by a method usually used using an excipient
usually used in the art, i.e., a pharmaceutical excipient, a pharmaceutical carrier, or the like.
Examples of the dosage forms of these pharmaceutical compositions include parenteral
agents such as injections and agents for drip infusion. Administration can be performedby
intravenous injection, subcutaneous injection, intravesical administration, or the like. For
the formulation, an excipient, a carrier, an additive, or the like suitable for these dosage forms can be used in a pharmaceutically acceptable range.
[0146] The amount of the conjugate of the present invention added for the formulation described above differs depending on the degree of symptoms or age of a patient, the dosage
form of a preparation used, or the binding titer of the Fab fragment, etc. For example, approximately 0.001 mg/kg to 100 mg/kg based on the mass of the Fab fragment can be used
per unit body weight of a patient.
[0147] The pharmaceutical composition comprising the conjugate of the present invention can be used for the treatment of a cancer. The cancer expected to be able to be treated by the pharmaceutical composition comprising the conjugate of the present invention is a cancer
expressing human MUC1. Examples thereof include breast cancer, lung cancer, colorectal cancer, bladder cancer, skin cancer, thyroid gland cancer, stomach cancer, pancreatic cancer, kidney cancer, ovary cancer and uterine cervical cancer.
[0148] A certain embodiment of the pharmaceutical composition comprising the conjugate
of the present invention is a pharmaceutical composition comprising the conjugate comprising a fluorescent dye and can be used in the treatment of a cancer by application to a
photoinimunotherapy method. The photoimmunotherapy method is a method of allowing
the conjugate comprising a fluorescent dye to specifically accumulate in cancer tissues,
followed by irradiation with light having a wavelength exciting the fluorescent dye contained
in the conjugate to induce cell death in a cancer-specific manner through the phototoxic
effect of the fluorescent dye. In the case of using the conjugate of the present invention
comprising a fluorescent dye in the photoimmunotherapy method, the wavelength of the light
for irradiation can be a near-infrared wavelength (650 to 1000 nm).
[0149] The present invention includes a pharmaceutical composition for treating breast
cancer or bladder cancer, comprising the conjugate of the present invention. The present invention also includes a method for treating breast cancer or bladder cancer, comprising the step of administering a therapeutically effective amount of the conjugate of the present invention, which can comprise the step of performing irradiation with light having a near infrared wavelength (650 to 1000 nm, for example, 660 to 740 nm, for example, 680 nm), in addition to the step described above. A certain embodiment of the dose of light irradiation isatleast1J/cm2 . A certain embodiment is at least 10 J/cm2 . A certain embodiment is at least100J/cm 2. A certain embodiment is 1to 500 J/cm2 . A certain embodiment is 50 to
200 J/cm 2 . In a certain embodiment, the irradiation may be carried out a plurality of times
after administration of the conjugate of the present invention. The present invention also
includes a method for inducing the cell death of cancer cells of breast cancer or bladder
cancer, comprising the step of administering a therapeutically effective amount of the
conjugate of the present invention.
[0150] The pharmaceutical composition for treating a cancer can also be used in the
diagnosis of a cancer. For example, the pharmaceutical composition for treating breast
cancer or bladder cancer can also be used in the diagnosis of the cancer.
[0151] The present invention also includes the conjugate of the present invention for use in
the treatment of breast cancer or bladder cancer. The present invention further includes use
of the conjugate of the present invention for the production of a pharmaceutical composition
for treating breast cancer or bladder cancer.
[0152] In an alternative embodiment, the present invention also relates to use of the anti
human MUC antibody Fab fragment of the present invention for the production of a
pharmaceutical composition comprising the conjugate of the present invention.
[0153] The present invention is generally described above. Particular Examples will be
provided here for reference in order to obtain further understanding. However, these are
given for illustrative purposes and do not limit the present invention.
EXAMPLES
[0154] (Example 1: Preparation of anti-human MUC1 antibody Fab fragment)
Two anti-human MUC Iantibody Fab fragments designated as P10-1 Fab and P10-2
Fab were prepared.
[0155] The amino acid sequences of the heavy chain variable regions and the light chain variable regions of P10-1 Fab and P10-2 Fab were specifically designed as sequences
expected to improve affinity and not to attenuate affinity even by the binding of a labeling
moiety, by using a molecular model of a humanized antibody constructed in accordance with
the literature (Proteins, 2014 Aug; 82 (8): 1624-35) after humanization of a1B2 antibody,
which is a mouse-derived anti-human cancer-specific MUC1 antibody, with reference to the method described in the literature (Front Biosci., 2008 Jan 1; 13: 1619-33).
[0156] GS vector pEE6.4 (Lonza Ltd.) having an insert of a heavy chain fragment gene
formed by connecting a gene encoding a signal sequence (MEWSWVFLFFLSVTTGVHS (SEQ ID NO: 13)) to the 5' side of the heavy chain variable region gene of P10-1 Fab or P10 2 Fab and connecting a human Igyl constant region gene (consisting of a nucleotide sequence
from nucleotide positions 355 to 669 of SEQ ID NO: 1 or 3) to the 3'side thereof was prepared. Here, in order to express each Fab fragment, a strop codon was inserted to
downstream of a codon of Asp at position 221 based on the EU index provided by Kabat et
al. (corresponding to Asp at position 222 in the amino acid sequences of SEQ ID NOs: 2 and
4 mentioned later) in the heavy chain constant region gene. Also, GS vector pEE12.4
(Lonza Ltd.) having an insert of a light chain gene formed by connecting a gene encoding a signal sequence (MSVPTQVLGLLLLWLTDARC (SEQ ID NO: 14)) to the 5' side of the
common light chain variable region gene of P10-1 Fab and P10-2 Fab and connecting a
human ic chain constant region gene (consisting of a nucleotide sequence from nucleotide
positions 340 to 660 of SEQ ID NO: 5) to the 3' side thereof was prepared.
[0157] The expression of each Fab fragment was performed by the method of transient expression. Expi293F cells (Thermo Fisher Scientific Inc.) cultured into approximately
2500000 cells/mL in Expi293 Expression Medium (Thermo Fisher Scientific Inc.) were
transfected with the GS vectors of the heavy chain fragment and the light chain mentioned
above using ExpiFectamine 293 Transfection Kit (Thermo Fisher Scientific Inc.), and
cultured for 8 days. After expression, the culture supernatant was purified using
KappaSelect (GE Healthcare Japan Corp.) to obtain each Fab fragment.
[0158] The nucleotide sequence of the heavy chain fragment of P10-1 Fab is shown in SEQ
ID NO: 1, and the amino acid sequence encoded thereby is shown in SEQ ID NO: 2. The
nucleotide sequence of the heavy chain variable region of P10-1 Fab is shown in SEQ ID
NO: 7. The amino acid sequence encoded thereby is shown in SEQ ID NO: 8.
[0159] The nucleotide sequence of the heavy chain fragment of P10-2 Fab is shown in SEQ
IDNO:3. The amino acid sequence encoded thereby is shown in SEQ ID NO: 4. The
nucleotide sequence of the heavy chain variable region of P10-2 Fab is shown in SEQ ID
NO: 9. The amino acid sequence encoded thereby is shown in SEQ ID NO: 10.
[0160] The light chain is common in P10-1 Fab and P10-2 Fab. The nucleotide sequence
thereof is shown in SEQ ID NO: 5. The amino acid sequence encoded thereby is shown in
SEQIDNO:6. The nucleotide sequence of the light chain variable region of P10-1 Fab and
P10-2 Fab is shown in SEQ ID NO: 11. The amino acid sequence encoded thereby is
shown in SEQ ID NO: 12.
[0161] (Example 2: Amino acid modification analysis of Fab fragment)
As a result of analyzing the amino acid modification of purified P10-2 Fab, it was
suggested that heavy chain N-terminal glutamine was modified into pyroglutamic acid in a
great majority of purified antibodies.
[0162] (Example 3: Binding activity evaluation of Fab fragment)
Binding activity against human cancer-specific MUC 1was compared as to P10-1
Fab and P10-2 Fab expressed by the method mentioned above with a chimeric 1B2 antibody
Fab fragment (hereinafter, referred to as 1B2 Fab; prepared by linking a human IgG1 CHi
domain and a K chain CL domain to the VH domain and the VL domain (their sequence
information was quoted from Patent Literature 1), respectively, of the 1B2 antibody (Patent
Literature 1); for the convenience of linking of the CHI domain and the CL domain, an
alanine residue at position 113 based on the EU index (Kabat et al.) in the VH domain was
substituted by a serine residue, and an alanine residue at position 109 based on the EU index
(Kabat et al.) in the VL domain was substituted by a threonine residue) by Cell ELISA.
Specifically, breast cancer cell line T-47D cells (purchasable from ATCC; HTB-133)
expressing human cancer-specific MUC were inoculated at 0.75 x 104 cells per well to a 96
well ELISA plate coated with collagen I, and cultured overnight. Then, the cells were fixed
in formalin, and P10-1 Fab, P10-2 Fab or 1B2 Fab described above was reacted therewith.
Then, a horseradish peroxidase (HRP)-labeled goat anti-human IgK antibody (Southern Biotechnology Associates, Inc.) was reacted as a secondary antibody. ECL Prime Western
Blotting Detection Reagent (GE Healthcare Japan Corp.) was added thereto for
luminescence, and the degree of the luminescence was examined. As a result, as shown in
Fig. 1, P10-1 Fab and P10-2 Fab were confirmed to have approximately 10 or more times the
binding activity against human cancer-specific MUCi compared to 1B2 Fab.
[0163] (Example 4: Fluorescent labeling of Fab fragment) Subsequently, the present inventors labeled P10-1 Fab, P10-2 Fab and 1B2 Fab with
a fluorescent dye mentioned above.
[0164] Specifically, each Fab fragment solution adjusted to approximately 1 mg/mL with
phosphate-buffered saline (pH 7.4) was adjusted to pH 8.5 by the addition of a 1/10 amount
of a 1 M dipotassium hydrogen phosphate solution (pH 9). IRDye800CW NHS Ester (LI COR Bioscience, Inc.) was added thereto at a final concentration of 310.8 pg/mL, and the
resultant was stirred at room temperature under shading for 2 hours. IRDye800CW NHS
Ester has a N-hydroxysuccinimide group and therefore reacts immediately with Lys of the
Fab fragment. This was recovered through Amicon Ultra 3K-0.5 mL centrifugal filter
(Merck Millipore) to purify a fluorescently labeled Fab fragment. P10-1Fab,P10-2Fab
and 1B2 Fab harboring this fluorescent dye were designated as P10-1 Fab Dye, P10-2 Fab
Dye and 1B2 Fab Dye.
[0165] (Example 5: Binding activity evaluation of fluorescently labeled Fab fragment) Binding activity against human cancer-specific MUC1 was compared as to P10-1
Fab Dye and P10-2 Fab Dye labeled by the method mentioned above with 1B2 Fab Dye by
Cell ELISA. Specifically, breast cancer cell line T-47D cells expressing human cancer
specific MUCL were inoculated at 0.75 x 104 cells per well to a 96-well ELISA plate coated with collagen I, and cultured overnight. Then, the cells were fixed in formalin, and P10-1
Fab Dye, P10-2 Fab Dye or1B2 Fab Dye described above was reacted therewith. Then,a
HRP-labeled goat anti-human Igx antibody (Southern Biotechnology Associates, Inc.) was reacted as a secondary antibody. ECL Prime Western Blotting Detection Reagent (GE
Healthcare Japan Corp.) was added thereto for luminescence, and the degree of the
luminescence was examined. Asa result, as shown in Fig. 2, the binding activity of1B2 Fab Dye was attenuated by labeling, whereas P10-1 Fab Dye and P10-2 Fab Dye were
confirmed to be free from the attenuation of the binding activity by labeling.
[0166] (Example 6: Labeling of Fab fragment with chelating agent)
Subsequently, the present inventors labeled P10-2 Fab with a chelating agent mentioned above.
[0167] Specifically, a Fab fragment solution adjusted to 12.5 mg/mL with phosphate
buffered saline (pH 7.4) was adjusted to pH 9.0 by the addition of a 100 M sodium carbonate
solutionat10mM. p-SCN-Bn-deferoxamine (Macrocyclics, Inc.) was added thereto at a final concentration of 1 mM, and the resultant was reacted at 37°C for 2 hours. p-SCN-Bn
deferoxamine has an isothiocyanate group and therefore reacts immediately with Lys of the
Fabfragment. This was recovered through Amicon Ultra 1OK-0.5 mL centrifugal filter to purify achelating agent-labeled Fab fragment. This chelating agent-labeled P10-2 Fab was
designated as P10-2 Fab DFO.
[0168] (Example 7: Binding activity evaluation of chelating agent-labeled Fab fragment) Binding activity against human cancer-specific MUC Iwas compared as to P10-2
Fab DFO labeled by the method mentioned above with P10-2 Fab by Cell ELISA.
Specifically, T-47D cells expressing human cancer-specific MUCi were inoculated at 0.75 x
104 cells to a 96-well ELISA plate coated with collagen I, and cultured overnight. Then, the
cells were fixed in formalin, and P10-2 Fab DFO or P10-2 Fab described above was reacted
therewith. Then, a HRP-labeled goat anti-human IgK antibody (Southern Biotechnology
Associates, Inc.) was reacted as a secondary antibody. ECL Prime Western Blotting
Detection Reagent (GE Healthcare Japan Corp.) was added thereto for luminescence, and the degree of the luminescence was examined. As aresult, as shown in Fig. 3, P10-2 Fab DFO and P10-2 Fab had equivalent binding activity. P10-2 Fab was confirmedtobe free from the attenuation of the binding activity by labeling with a chelating agent.
[0169] (Example 8: Reactivity of P10-2 inhuman bladder cancer tissue sample)
In order to study the reactivity of P10-2 Fab in human bladder cancer, the study was
made by immunostaining using a human bladder cancer tissue array (US Biomax, Inc., BC12011b). When P10-2 Fab is used as a primary antibody, an anti-human antibody used
as a secondary antibody cross-reacts with human tissues. Therefore, mouse chimeric P10-2 IgG (antibody in which the VH domain and the VL domain of P10-2 Fab were fused with
mouse IgG2a CH Ito CH3 domains and a mouse - chain CL domain, respectively) was prepared and used as a primary antibody. The human bladder cancer tissue array sample
was reacted with a 3% hydrogen peroxide solution for 5 minutes and then washed with phosphate-buffered saline of pH 7.4. Then, mouse chimeric P10-2 IgG (0.25 pg/mL) was
reacted, and then, One-Step Polymer-HRP antibody (BioGenex) was reacted as a secondary antibody. Super Sensitive DAB (BioGenex) was added thereto for color development.
The positive reaction of staining for cancer tissues was determined as ±: very mildly positive, +: positive, ++: moderately positive, and +++: highly positive, and one case whose cancer
tissues were not clear was excluded. As a result, positive reaction was found in 57 out of 59
studied cases with 11 cases for ±, 24 cases for +, 17 cases for ++, and 5 cases for+++
(positive rate: 97%).
[0170] (Example 9: Labeling of chelated Fab fragment with 89Zr)
89Zr used was dissolved in a 1 M aqueous oxalic acid solution and produced as '9Z
Oxalate (Okayama University). 20 pL of 89Zr-Oxalate (21.4 MBq) was neutralized with 10
pL of a 2 M aqueous sodium carbonate solution. Then, 70 pL of a 5 mg/mL solution of
gentisic acid dissolved in 250 mM aqueous sodium acetate solution was added thereto.
Further, 200 pL of a 500 mM aqueous HEPES (4-(2-hydroxyethyl)-1
piperazineethanesulfonic acid) solution containing 0.1% polysorbate 80 and 20% glycerol was added thereto. To this solution containing 8 9Zr, 100 pL of 9.5 mg/mL P10-2 Fab DFO was added and reacted at room temperature for 30 minutes. The obtained reaction mixture was purified using Amicon Ultra 1OK-0.5 mL centrifugal filter (Merck Millipore) and further filtered through a membrane filter (Millex-GV 0.22 pm 13 mm; Merck Millipore) to obtain 8 9Zr-labeledP10-2 Fab DFO (16.1 MBq) of interest. This 89Zr-labeledP10-2 Fab DFO was designated as P10-2 Fab DFO 89Zr. The obtained P10-2 Fab DFO 89Zr solution was analyzed using high-performance liquid chromatography (20AD series; Shimadzu Corp.).
The retention time (UV: 10.192 min) of P10-2 Fab DFO was compared with the retention time (UV: 10.178 min, RI: 10.515 min) of P10-2 Fab DFO8 9Zr. The respective retention times were equivalent, confirming that P10-2 Fab DFO was labeled with8 9Zr. TheHPLC
analysis was carried out under the following conditions: column: BioSep SEC s3000 300 x
7.8 mm (Phenomenex Inc.), column temperature: room temperature, UV detector wavelength: 280 nm, mobile phase: phosphate buffer solution (Gibco, 10010-023), flow rate:
1 mL/min.
[0171] (Example 10: Labeling of Fab fragment with IRDye700DX)
IRDye700DX NHS Ester (LI-COR Bioscience, Inc.) was used to label P10-2
Fabwith IRDye700DX.
[0172] Specifically, a P10-2 Fab solution adjusted to 1 mg/mL with phosphate-buffered
saline (pH 7.4) was supplemented with a 1/10 amount of a 1 M dipotassium hydrogen
phosphate solution (pH 9). IRDye700DX NHS Ester was added thereto at a final
concentration of 154 pg/mL, and the resultant was stirred at room temperature for 2 hours.
After reaction, IRDye700DX-labeled P10-2 Fab was purified by recovery through Amicon
Ultra 10K-15 mL centrifugal filter (Merck Millipore). This IRDye700DX-labeledP10-2
Fab was designated as P10-2 Fab IR700.
[0173] (Example 11: Binding activity evaluation of Fab fragment against breast cancer cell line and bladder cancer cell line)
The binding activity of P10-2 Fab in human breast cancer and bladder cancer was
studied.
[0174] Specifically, human breast cancer cell line MDA-MB-468 cells (purchasable from
ATCC; HTB-132; hereinafter, referred to as MM-468 cells) or human bladder cancer cell line
647-V cells (purchasable from DSMZ; ACC 414) expressing human cancer-specific MUCI were inoculated at I x 10 4 cells per well to a 96-well ELISA plate and cultured overnight.
Then, P10-2 Fab described above was reacted at a concentration of 0.0000003 to 0.001 mg/mL. Then, a horseradish peroxidase (HRP)-labeled goat anti-human IgG antibody
(Medical & Biological Laboratories Co., Ltd.) was reacted as a secondary antibody. ECL
Prime Western Blotting Detection Reagent (GE Healthcare Japan Corp.) was added thereto
for luminescence, and the degree of the luminescence was examined. As a result, as shown
in Fig. 4, P10-2 Fab was found to have binding activity against the human breast cancer cell
line MM-468 cells and the human bladder cancer cell line 647-V cells.
[0175] (Example 12: Contrast evaluation of fluorescently labeled Fab fragment in
subcutaneously cancer-bearing model) 3 x 106 human breast cancer cell line MM-468 cells were subcutaneously
transplanted as human cancer-specific MUC1-positive cells to the right back of each
immunodeficient mouse (SCID mouse; Charles River Laboratories Japan, Inc.). Mice having tumorigenesis were selected approximately one month after the transplantation.
P10-2 Fab Dye dissolved in phosphate-buffered saline (pH 7.4) was intravenously administered at a dose of 0.1, 0.3, 1 or 3 mg/kg (N = 2 for the 0.1 mg/kg administration
group, and N = 3 for the 0.3, 1 and 3 mg/kg administration groups). Photographs were
taken with a usual camera and a near-infrared fluorescence camera (Fluobeam (800 nm
filter); Fluoptics) 6 hours and 24 hours after the P10-2 Fab Dye administration. The
fluorescent brightness of a tumor site and a peritumoral background site in the image taken
with the infrared fluorescence camera was measured. Asa result, as shown inFig. 5A, P10
2 Fab Dye was found to accumulate in the human cancer-specific MUC-positive MM-468
tumor site and be clearly visible in the fluorescent image 6 hours after administration. As
shown in Fig. 5B, the tumor/background ratio was found to elevate in a P10-2 Fab Dye dose
dependent manner in the range of 0.1 to 3 mg/kg. It was further obvious that the effect was
sustained even 24 hours after administration. These results demonstrated that P10-2 Fab
Dye permits detection of human MUC1--positive cancer cells from 6 hours to 24 hours after
administration.
[0176] (Example 13: Detection of tumor with IRDye700DX labeled Fab fragment)
5x 106 MM-468 cells were subcutaneously transplanted to the right back of each
immunodeficient mouse (nude mouse; Charles River Laboratories Japan, Inc.). This test
was conducted atN=2. P10-2 Fab IR700 (3 mg/kg) or a vehicle (phosphate-buffered
saline) was intravenously administered 40 days after the transplantation. The animals were
euthanized 2 hours after the P10-2 Fab IR700 administration. Tumor was excised, and the
luminescence of the tumor sites was measured by excitation at a wavelength of 675 nm and
detection at a wavelength of 740 nm in IVIS SPECTRUM (PerkinElmer, Inc.). As a result,
as shown in Fig. 6, P10-2 Fab IR700 was found to accumulate in MM-468 cells 2 hours after
administration.
[0177] (Example 14: Cytotoxicity evaluation of IRDye700DX labeled Fab fragment)
In order to study the utilization of P10-2 Fab IR700 in cancer treatment, cytotoxicity
in photoimmunotherapy was evaluated.
[0178] Specifically, human breast cancer cell line MM-468 cells, human bladder cancer cell
line 647-V cells or CHO-K1 cells of Comparative Example (purchasable from ATCC; CCL
61) were inoculated at 5 x 103 cells per well to a 384-well white plate and cultured overnight.
Then, P10-2 Fab IR700 was reacted at 0, 0.01, 0.1, or 1 tg/mL and then irradiated with 0 to
30 J/cm 2 of light having a wavelength of 680 nm. After the light irradiation, overnight
culture was performed. CellTiter-Glo (Promega Corp.) was added thereto for luminescence,
and the luminescence was measured to measure the number of live cells. This test was
conducted using 3 wells under each condition. As a result, as shown in Fig. 7, it was
obvious that P10-2 Fab IR700 exhibits cytotoxicity in a manner specific for the expression of
human cancer-specific MUC1 by light irradiation.
[0179] (Example 15: Antitumor activity evaluation of IRDye700DX labeled Fab fragment)
5x 106 MM-468 cells were subcutaneously transplanted to the right back of each
immunodeficient mouse (nude mouse; Charles River Laboratories Japan, Inc.). This test was conducted at N = 4. After tumor volume became 300 mm 3 , P10-2 Fab IR700 (0.3, 1, or
3 mg/kg) was intravenously administered at days 1, 5, 8, 12 and 15. Phosphate-buffered saline was similarly administered to a vehicle group. On the day following the drug
administration, irradiation with 0 or 200 J/cm2 of light having a wavelength of 680 nm was
performed, and the tumor volume was measured over time. As a result, as shown in Fig. 8, it was obvious that P10-2 Fab IR700 showed an antitumor effect in a manner dependent on a
dose and light irradiation.
INDUSTRIAL APPLICABILITY
[0180] The anti-human MUCI antibody Fab fragment of the present invention is expected to be useful in the diagnosis and/or treatment of cancers such as breast cancer, lung cancer,
colorectal cancer, bladder cancer, skin cancer, thyroid gland cancer, stomach cancer,
pancreatic cancer, kidney cancer, ovary cancer or uterine cervical cancer.
SEQUENCE LISTING FREE TEXT
[0181] SEQ ID NO: 1: Nucleotide sequence of DNA encoding a P10-1 Fab heavy chain
fragment SEQ ID NO: 2: Amino acid sequence of the P10-1 Fab heavy chain fragment
SEQ ID NO: 3: Nucleotide sequence of DNA encoding a P10-2 Fab heavy chain fragment
SEQ ID NO: 4: Amino acid sequence of the P10-2 Fab heavy chain fragment
SEQ ID NO: 5: Nucleotide sequence of DNA encoding an antibody light chain
SEQ ID NO: 6: Amino acid sequence of the antibody light chain
SEQ ID NO: 7: Nucleotide sequence of DNA encoding a P10-1 Fab heavy chain
variable region
SEQ ID NO: 8: Amino acid sequence of the P10-1 Fab heavy chain variable region
SEQ ID NO: 9: Nucleotide sequence of DNA encoding a P10-2 Fab heavy chain
variable region
SEQ ID NO: 10: Amino acid sequence of the P10-2 Fab heavy chain variable region
SEQ ID NO: 11: Nucleotide sequence of DNA encoding an antibody light chain variable region SEQ ID NO: 12: Amino acid sequence of the antibody light chain variable region SEQ ID NO: 13: Heavy chain signal sequence SEQ ID NO: 14: Light chain signal sequence SEQ ID NO: 15: Tandem repeat sequence of the extracellular domain ofMUCI
[0182] The reference in this specification to any prior publication (or information derived from it), or to any matter which is known, is not, and should not be taken as an acknowledgment or admission or any form of suggestion that that prior publication (or information derived from it) or known matter forms part of the common general knowledge in the field of endeavour to which this specification relates.
[0183] Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" and "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps.

Claims (52)

THE CLAIMS DEFINING THE INVENTION ARE AS FOLLOWS:
1. An anti-human MUC1 antibody Fab fragment selected from the group consisting of the following (a) and (b): (a) an anti-human MUC1 antibody Fab fragment comprising a heavy chain fragment comprising a heavy chain variable region consisting of the amino acid sequence represented by SEQ ID NO: 8 or SEQ ID NO: 10 and a light chain comprising a light chain variable region consisting of the amino acid sequence represented by SEQ ID NO: 12; and (b) an anti-human MUC Iantibody Fab fragment comprising a heavy chain fragment comprising a heavy chain variable region derived from a heavy chain variable region consisting of the amino acid sequence represented by SEQ ID NO: 8 or SEQ ID NO: 10 by the modification of glutamine at amino acid position 1 of SEQ ID NO: 8 or SEQ ID NO: 10 into pyroglutamic acid, and a light chain comprising a light chain variable region consisting of the amino acid sequence represented by SEQ ID NO: 12.
2. The anti-human MUC Iantibody Fab fragment according to claim 1 which is selected from the group consisting of the following (a) and (b): (a) an anti-human MUC1 antibody Fab fragment comprising a heavy chain fragment consisting of the amino acid sequence represented by SEQ ID NO: 2 or SEQ ID NO: 4 and a light chain consisting of the amino acid sequence represented by SEQ ID NO: 6; and (b) an anti-human MUC Iantibody Fab fragment comprising a heavy chain fragment derived from a heavy chain fragment consisting of the amino acid sequence represented by SEQ ID NO: 2 or SEQ ID NO: 4 by the modification of glutamine at amino acid position 1 of SEQ ID NO: 2 or SEQ ID NO: 4 into pyroglutamic acid, and a light chain consisting of the amino acid sequence represented by SEQ ID NO: 6.
3. The anti-human MUC Iantibody Fab fragment according to claim 1 which is selected from the group consisting of the following (a) and (b): (a) an anti-human MUC1 antibody Fab fragment comprising a heavy chain fragment comprising a heavy chain variable region consisting of the amino acid sequence represented by SEQ ID NO: 10 and a light chain comprising a light chain variable region consisting of the amino acid sequence represented by SEQ ID NO: 12; and (b) an anti-human MUC Iantibody Fab fragment comprising a heavy chain fragment comprising a heavy chain variable region derived from a heavy chain variable region consisting of the amino acid sequence represented by SEQ ID NO: 10 by the modification of glutamine at amino acid position 1 of SEQ ID NO: 10 into pyroglutamic acid, and a light chain comprising a light chain variable region consisting of the amino acid sequence represented by SEQ ID NO: 12.
4. The anti-human MUC Iantibody Fab fragment according to claim 3 which is selected from the group consisting of the following (a) and (b): (a) an anti-human MUC1 antibody Fab fragment comprising a heavy chain fragment consisting of the amino acid sequence represented by SEQ ID NO: 4 and a light chain consisting of the amino acid sequence represented by SEQ ID NO: 6; and (b) an anti-human MUC Iantibody Fab fragment comprising a heavy chain fragment derived from a heavy chain fragment consisting of the amino acid sequence represented by SEQ ID NO: 4 by the modification of glutamine at amino acid position 1 of SEQ ID NO: 4 into pyroglutamic acid, and a light chain consisting of the amino acid sequence represented by SEQ ID NO: 6.
5. The anti-human MUC Iantibody Fab fragment according to claim 4 which is an anti-human MUC1 antibody Fab fragment comprising a heavy chain fragment consisting of the amino acid sequence represented by SEQ ID NO: 4 and a light chain consisting of the amino acid sequence represented by SEQ ID NO: 6.
6. The anti-human MUC Iantibody Fab fragment according to claim 4 which is an anti-human MUC1 antibody Fab fragment comprising a heavy chain fragment derived from a heavy chain fragment consisting of the amino acid sequence represented by SEQ ID NO: 4 by the modification of glutamine at amino acid position 1 of SEQ ID NO: 4 into pyroglutamic acid, and a light chain consisting of the amino acid sequence represented by SEQ ID NO: 6.
7. A conjugate comprising one or more labeling moiety and the anti-human
MUC Iantibody Fab fragment according to any one of claims I to 6.
8. The conjugate according to claim 7, wherein the labeling moiety is (i) a ligand and a linker, (ii) a ligand, (iii) a fluorescent dye and a linker, or (iv) a fluorescent dye.
9. The conjugate according to claim 8, wherein the labeling moiety is (i) a ligand and a linker or (ii) a ligand.
10. The conjugate according to claim 9, wherein the ligand is a ligand represented by the following formula (A):
[Chemical Formula 1]
H NH N N
OH NO (A) o NH 3
O2W'N H
H H wherein the wavy line represents binding to the anti-human MUC1 antibody Fab fragment or the linker.
11. The conjugate according to claim 10, wherein the labeling moiety is a ligand and a linker represented by the following formula (A'):
[Chemical Formula 2]
0
OH NH N
O O
N'OHNA' O NH HC_ H 3C 0 H S ON
O N N I H H OH wherein the wavy line represents binding to the anti-human MUC1 antibody Fab fragment.
12. The conjugate according to claim 11, wherein the anti-human MUC Iantibody Fab fragment is bound via an amino group thereof to the carbon atom of a labeling moiety terminal C(=S) group.
13. A conjugate selected from the group consisting of the following (a) to (c): (a) the conjugate according to claim 12 wherein the anti-human MUC1 antibody Fab fragment is the anti-human MUC1 antibody Fab fragment according to claim 5; (b) the conjugate according to claim 12 wherein the anti-human MUC1 antibody Fab fragment is the anti-human MUC1 antibody Fab fragment according to claim 6; and (c) a conjugate which is a mixture of (a) and (b).
14. The conjugate according to any one of claims 9 to 13, further comprising a metal.
15. The conjugate according to claim 14, wherein the metal is a metal radioisotope.
16. The conjugate according to claim 15, wherein the metal is 89Zr.
89Zr. 17. The conjugate according to claim 13, further comprising
18. The conjugate according to claim 8, wherein the labeling moiety is (i) a fluorescent dye and a linker or (ii) a fluorescent dye.
19. The conjugate according to claim 18, wherein the fluorescent dye is a fluorescent dye selected from the group consisting of the following formula (B) and the following formula (C):
[Chemical Formula 3]
SO 3Na
NaO3S SO3~
N N+
SO 3 Na O C (B)
[Chemical Formula 4]
SO 3 Na
O /' o_ Nt .-,XSO3~ HN 0 O N N N SO 3Na
N--Si--N
NN N
=O N0a
(C) wherein the wavy line represents binding to the anti-human MUC1 antibody Fab fragment or the linker.
20. The conjugate according to claim 19, wherein the wavy line represents binding to the anti-human MUC1 antibody Fab fragment, and the anti-human MUC1 antibody Fab fragment is bound via an amino group thereof to the carbon atom of a labeling moiety terminal C(=O) group.
21. The conjugate according to claim 20, wherein the labeling moiety is a fluorescent dye represented by formula (B).
22. A conjugate selected from the group consisting of the following (a) to (c): (a) the conjugate according to claim 21 wherein the anti-human MUC1 antibody Fab fragment is the anti-human MUC Iantibody Fab fragment according to claim 5; (b) the conjugate according to claim 21 wherein the anti-human MUC1 antibody Fab fragment is the anti-human MUC1 antibody Fab fragment according to claim 6; and (c) a conjugate which is a mixture of (a) and (b).
23. The conjugate according to claim 20, wherein the labeling moiety is a fluorescent dye represented by formula (C).
24. A conjugate selected from the group consisting of the following (a) to (c): (a) the conjugate according to claim 23 wherein the anti-human MUC1 antibody Fab fragment is the anti-human MUC1 antibody Fab fragment according to claim 5; (b) the conjugate according to claim 23 wherein the anti-human MUC1 antibody Fab fragment is the anti-human MUC1 antibody Fab fragment according to claim 6; and (c) a conjugate which is a mixture of (a) and (b).
25. A polynucleotide comprising the following (a) and (b): (a) a polynucleotide comprising a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC1 antibody Fab fragment according to claim 1; and (b) a polynucleotide comprising a nucleotide sequence encoding the light chain of the anti-human MUC1 antibody Fab fragment according to claim 1.
26. A polynucleotide comprising the following (a) and (b):
(a) a polynucleotide comprising a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC Iantibody Fab fragment according to claim 5; and (b) a polynucleotide comprising a nucleotide sequence encoding the light chain of the anti-human MUC1 antibody Fab fragment according to claim 5.
27. An expression vector comprising the following (a) and (b): (a) a polynucleotide comprising a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC1 antibody Fab fragment according to claim 1; and (b) a polynucleotide comprising a nucleotide sequence encoding the light chain of the anti-human MUC1 antibody Fab fragment according to claim 1.
28. An expression vector comprising the following (a) and (b): (a) a polynucleotide comprising a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC Iantibody Fab fragment according to claim 5; and (b) a polynucleotide comprising a nucleotide sequence encoding the light chain of the anti-human MUC1 antibody Fab fragment according to claim 5.
29. A host cell selected from the group consisting of the following (a) to (b): (a) a host cell transformed with an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC1 antibody Fab fragment according to claim 1 and a polynucleotide comprising a nucleotide sequence encoding the light chain of the anti-human MUC1 antibody Fab fragment according to claim 1; and (b) a host cell transformed with an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC1 antibody Fab fragment according to claim 1 and an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding the light chain of the anti-human MUC1 antibody Fab fragment according to claim 1.
30. A host cell selected from the group consisting of the following (a) to (b): (a) a host cell transformed with an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC Iantibody Fab fragment according to claim 5 and a polynucleotide comprising a nucleotide sequence encoding the light chain of the anti-human MUC1 antibody Fab fragment according to claim 5; and (b) a host cell transformed with an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC1 antibody Fab fragment according to claim 5 and an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding the light chain of the anti-human MUC1 antibody Fab fragment according to claim 5.
31. A method for producing an anti-human MUC1 antibody Fab fragment comprising the step of culturing a host cell selected from the group consisting of the following (a) to (c) to express the anti-human MUC1 antibody Fab fragment: (a) a host cell transformed with an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC Iantibody Fab fragment according to claim 1 and a polynucleotide comprising a nucleotide sequence encoding the light chain of the anti-human MUC1 antibody Fab fragment according to claim 1; (b) a host cell transformed with an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC1 antibody Fab fragment according to claim 1 and an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding the light chain of the anti-human MUC1 antibody Fab fragment according to claim 1; and (c) a host cell transformed with an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC1 antibody Fab fragment according to claim 1, and a host cell transformed with an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding the light chain of the anti-human MUC1 antibody Fab fragment according to claim 1.
32. A method for producing an anti-human MUC1 antibody Fab fragment comprising the step of culturing a host cell selected from the group consisting of the following (a) to (c) to express the anti-human MUC1 antibody Fab fragment: (a) a host cell transformed with an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC Iantibody Fab fragment according to claim 5 and a polynucleotide comprising a nucleotide sequence encoding the light chain of the anti-human MUC1 antibody Fab fragment according to claim 5; (b) a host cell transformed with an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC1 antibody Fab fragment according to claim 5 and an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding the light chain of the anti-human MUC1 antibody Fab fragment according to claim 5; and (c) a host cell transformed with an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding the heavy chain fragment of the anti-human MUC Iantibody Fab fragment according to claim 5, and a host cell transformed with an expression vector comprising a polynucleotide comprising a nucleotide sequence encoding the light chain of the anti-human MUC1 antibody Fab fragment according to claim 5.
33. A method for producing a conjugate comprising a labeling moiety and an anti human MUC1 antibody Fab fragment, comprising the steps of: producing the anti human MUC1 antibody Fab fragment by the method according to claim 31 or 32; and covalently binding the Fab fragment to the labeling moiety.
34. The method for producing a conjugate according to claim 33, wherein the step of covalently binding the Fab fragment to the labeling moiety is the step of i) binding the Fab fragment via a linker to a ligand or ii) covalently binding the Fab fragment directly to a ligand.
35. The method for producing a conjugate according to claim 34, further comprising the step of labeling the ligand of the conjugate with a metal radioisotope.
36. The method for producing a conjugate according to claim 33, wherein the step of covalently binding the Fab fragment to the labeling moiety is the step of i) binding the Fab fragment via a linker to a fluorescent dye or ii) covalently binding the Fab fragment directly to a fluorescent dye.
37. A composition for diagnosis comprising one or more conjugate according to any of claims 7 to 24, and a pharmaceutically acceptable carrier.
38. The composition for diagnosis according to claim 37, wherein the conjugate is the conjugate according to any one of claims 17, 22 and 24.
39. The composition for diagnosis according to claim 38, wherein the conjugate is the conjugate according to claim 17.
40. The composition for diagnosis according to claim 38, wherein the conjugate is the conjugate according to claim 22.
41. The composition for diagnosis according to claim 38, wherein the conjugate is the conjugate according to claim 24.
42. The composition for diagnosis according to any one of claims 37 to 41 which is used in the diagnosis of a cancer expressing human MUC1.
43. The composition for diagnosis according to claim 42, wherein the cancer is breast cancer or bladder cancer.
44. A pharmaceutical composition comprising one or more conjugate according to any of claims 7 to 24, and a pharmaceutically acceptable carrier.
45. The pharmaceutical composition according to claim 44, wherein the conjugate is the conjugate according to any one of claims 17, 22 and 24.
46. The pharmaceutical composition according to claim 45, wherein the conjugate is the conjugate according to claim 24.
47. The pharmaceutical composition according to any one of claims 44 to 46 which is a pharmaceutical composition for treating a cancer expressing human MUC1.
48. The pharmaceutical composition according to claim 47, wherein the cancer is breast cancer or bladder cancer.
49. Use of the conjugate according to any one of claims 7 to 24 for the production of a composition for the diagnosis of breast cancer expressing human MUC1 or bladder cancer expressing human MUC1 and/or a pharmaceutical composition for treating breast cancer expressing human MUC Ior bladder cancer expressing human MUCI.
50. Use of the conjugate according to any one of claims 7 to 24 in the manufacture of a medicament for the diagnosis and/or treatment of breast cancer expressing human MUC1 or bladder cancer expressing human MUC1.
51. A method for diagnosing breast cancer expressing human MUC1 or bladder cancer expressing human MUC1, comprising preoperatively or intraoperatively administering the conjugate according to any one of claims 7 to 24 to a subject.
52. A method for treating breast cancer expressing human MUC Ior bladder cancer expressing human MUC1, comprising the step of administering a therapeutically effective amount of the conjugate according to any one of claims 7 to 24.
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